Yum, tasty mutations...

MutationTaster - study a chromosomal position

MTQE documentation
NEVER press reload or F5 - unless you want to start from the very beginning.
input seems to be ok - now mapping the variant to the different transcripts...
found 2 transcript(s)...
Querying Taster for transcript #1: ENST00000379802
Querying Taster for transcript #2: ENST00000418664
MT speed 0.39 s - this script 2.510093 s

Results


genesymbolpredictionprobabilitymodelprediction
problem
splicingClinVaramino acid changesvariant typedbSNP IDprotein lengthfile
DSPpolymorphism2.5139307202604e-07simple_aaeaffectedV30Msingle base exchangers121912998show file
DSPpolymorphism2.5139307202604e-07simple_aaeaffectedV30Msingle base exchangers121912998show file

Taster files

Yum, tasty mutations...

mutation t@sting

documentation

Prediction

polymorphism

Model: simple_aae, prob: 0.999999748606928      (explain)
Summary
  • amino acid sequence changed
  • heterozygous in TGP or ExAC
  • known as potential disease variant: rs16846 (probable pathogenic)
  • known disease mutation at this position (HGMD CM063961)
  • protein features (might be) affected
  • splice site changes
hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr6:7542236G>AN/A show variant in all transcripts   IGV
HGNC symbol DSP
Ensembl transcript ID ENST00000379802
Genbank transcript ID NM_004415
UniProt peptide P15924
alteration type single base exchange
alteration region CDS
DNA changes c.88G>A
cDNA.429G>A
g.429G>A
AA changes V30M Score: 21 explain score(s)
position(s) of altered AA
if AA alteration in CDS
30
frameshift no
known variant Reference ID: rs121912998
databasehomozygous (A/A)heterozygousallele carriers
1000G01111
ExAC1147148

known as potential disease variant: rs16846 (probable pathogenic for Cardiomyopathy|Right ventricular cardiomyopathy|Dilated cardiomyopathy with woolly hair and keratoderma|Arrhythmogenic right ventricular dysplasia 8|Skin fragility-woolly hair-palmoplantar keratoderma syndrome|Lethal acantholytic epidermolysis bullosa|Keratosis palmoplantaris striata II|Arrhythmogenic right ventricular cardiomyopathy|not specified|Cardiovascular phenotype|not provided) dbSNP  NCBI variation viewer
known disease mutation at this position, please check HGMD for details (HGMD ID CM063961)

known disease mutation at this position, please check HGMD for details (HGMD ID CM063961)
known disease mutation at this position, please check HGMD for details (HGMD ID CM063961)
regulatory features Promoter Associated, Regulatory Feature, Promoter like regulatory feature
H3K4me2, Histone, Histone 3 Lysine 4 Di-Methylation
H3K27me3, Histone, Histone 3 Lysine 27 Tri-Methylation
PolII, Polymerase, RNA Polymerase II
H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
H2AZ, Histone, Histone 2A variant Z
HEY1, Transcription Factor, HEY1 Transcription Factor Binding
H3K9ac, Histone, Histone 3 Lysine 9 Acetylation
H3K27ac, Histone, Histone 3 Lysine 27 Acetylation
TAF1, Transcription Factor, TAF1 Transcription Factor Binding
H3K4me3, Histone, Histone 3 Lysine 4 Tri-Methylation
DNase1, Open Chromatin, DNase1 Hypersensitive Site
phyloP / phastCons
PhyloPPhastCons
(flanking)1.3470.905
-2.50.304
(flanking)0.4260.518
explain score(s) and/or inspect your position(s) in in UCSC Genome Browser
splice sites
effectgDNA positionscorewt detection sequence exon-intron border
Donor increased425wt: 0.84 / mu: 0.99wt: CGCTACGAGGTGACC
mu: CGCTACGAGATGACC
 CTAC|gagg
Donor increased427wt: 0.45 / mu: 0.59wt: CTACGAGGTGACCAG
mu: CTACGAGATGACCAG
 ACGA|ggtg
Donor gained4300.32mu: CGAGATGACCAGCGG AGAT|gacc
distance from splice site 83
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      30RAESGPDLRYEVTSGGGGTSRMYY
mutated  all conserved    30RAESGPDLRYEMTSGGGGTSRMY
Ptroglodytes  all identical  ENSPTRG00000017702  30RAESGPDLRYEVTSGGGGTSRMY
Mmulatta  all conserved  ENSMMUG00000014784  30RAESGPDLRYEMTSGGGGTSRIY
Fcatus  no homologue    
Mmusculus  all conserved  ENSMUSG00000054889  30RAESGPDLRYEMTYSGGGGGGGGGGGGGTSRTF
Ggallus  all conserved  ENSGALG00000012790  30RADSGTDLRYEMSSHVVGGGGGGTHTHKTY
Trubripes  no homologue    
Drerio  no alignment  ENSDARG00000022309  n/a
Dmelanogaster  no homologue    
Celegans  no homologue    
Xtropicalis  no homologue    
protein features
start (aa)end (aa)featuredetails 
1584REGIONInteracts with plakophilin 1 and junction plakoglobin.lost
11056REGIONGlobular 1.lost
2828MOD_RESPhosphotyrosine.might get lost (downstream of altered splice site)
5656MOD_RESPhosphotyrosine.might get lost (downstream of altered splice site)
165165MOD_RESPhosphoserine.might get lost (downstream of altered splice site)
166166MOD_RESPhosphoserine.might get lost (downstream of altered splice site)
176176MOD_RESPhosphoserine.might get lost (downstream of altered splice site)
178178MOD_RESPhosphoserine.might get lost (downstream of altered splice site)
178271REPEATSpectrin 1.might get lost (downstream of altered splice site)
182201HELIXmight get lost (downstream of altered splice site)
211241HELIXmight get lost (downstream of altered splice site)
245294HELIXmight get lost (downstream of altered splice site)
272375REPEATSpectrin 2.might get lost (downstream of altered splice site)
307338HELIXmight get lost (downstream of altered splice site)
344402HELIXmight get lost (downstream of altered splice site)
376446REPEATSpectrin 3a.might get lost (downstream of altered splice site)
411442HELIXmight get lost (downstream of altered splice site)
447515DOMAINSH3.might get lost (downstream of altered splice site)
449451HELIXmight get lost (downstream of altered splice site)
462467STRANDmight get lost (downstream of altered splice site)
469471STRANDmight get lost (downstream of altered splice site)
474476STRANDmight get lost (downstream of altered splice site)
481486STRANDmight get lost (downstream of altered splice site)
488496STRANDmight get lost (downstream of altered splice site)
498500STRANDmight get lost (downstream of altered splice site)
503506STRANDmight get lost (downstream of altered splice site)
507509HELIXmight get lost (downstream of altered splice site)
516545REPEATSpectrin 3b.might get lost (downstream of altered splice site)
517561HELIXmight get lost (downstream of altered splice site)
546627REPEATSpectrin 4.might get lost (downstream of altered splice site)
565568HELIXmight get lost (downstream of altered splice site)
573575TURNmight get lost (downstream of altered splice site)
576594HELIXmight get lost (downstream of altered splice site)
602624HELIXmight get lost (downstream of altered splice site)
654769REPEATSpectrin 5.might get lost (downstream of altered splice site)
770883REPEATSpectrin 6.might get lost (downstream of altered splice site)
905905CONFLICTA -> R (in Ref. 1; AAA85135).might get lost (downstream of altered splice site)
10181945COILEDPotential.might get lost (downstream of altered splice site)
10571945REGIONCentral fibrous rod domain.might get lost (downstream of altered splice site)
11201120CONFLICTD -> R (in Ref. 4; AAA35766).might get lost (downstream of altered splice site)
12201220MOD_RESPhosphothreonine.might get lost (downstream of altered splice site)
12251225MOD_RESPhosphoserine.might get lost (downstream of altered splice site)
19462871REGIONGlobular 2.might get lost (downstream of altered splice site)
19602208REGION4.5 X 38 AA tandem repeats (Domain A).might get lost (downstream of altered splice site)
20092045REPEATPlectin 1.might get lost (downstream of altered splice site)
20242024MOD_RESPhosphoserine.might get lost (downstream of altered splice site)
20462083REPEATPlectin 2.might get lost (downstream of altered splice site)
20842121REPEATPlectin 3.might get lost (downstream of altered splice site)
21222159REPEATPlectin 4.might get lost (downstream of altered splice site)
21632197REPEATPlectin 5.might get lost (downstream of altered splice site)
21982233REPEATPlectin 6.might get lost (downstream of altered splice site)
22092209MOD_RESPhosphoserine.might get lost (downstream of altered splice site)
22132217STRANDmight get lost (downstream of altered splice site)
22192224HELIXmight get lost (downstream of altered splice site)
22302237HELIXmight get lost (downstream of altered splice site)
22442446REGION4.5 X 38 AA tandem repeats (Domain B).might get lost (downstream of altered splice site)
22462249HELIXmight get lost (downstream of altered splice site)
22512254HELIXmight get lost (downstream of altered splice site)
22512288REPEATPlectin 7.might get lost (downstream of altered splice site)
22602265STRANDmight get lost (downstream of altered splice site)
22662269TURNmight get lost (downstream of altered splice site)
22702273STRANDmight get lost (downstream of altered splice site)
22742278HELIXmight get lost (downstream of altered splice site)
22752275MOD_RESPhosphotyrosine.might get lost (downstream of altered splice site)
22792283STRANDmight get lost (downstream of altered splice site)
22852296HELIXmight get lost (downstream of altered splice site)
22892326REPEATPlectin 8.might get lost (downstream of altered splice site)
23012303STRANDmight get lost (downstream of altered splice site)
23042307TURNmight get lost (downstream of altered splice site)
23082310STRANDmight get lost (downstream of altered splice site)
23122317HELIXmight get lost (downstream of altered splice site)
23232333TURNmight get lost (downstream of altered splice site)
23272364REPEATPlectin 9.might get lost (downstream of altered splice site)
23342337HELIXmight get lost (downstream of altered splice site)
23422344TURNmight get lost (downstream of altered splice site)
23502354HELIXmight get lost (downstream of altered splice site)
23552357TURNmight get lost (downstream of altered splice site)
23612372HELIXmight get lost (downstream of altered splice site)
23652402REPEATPlectin 10.might get lost (downstream of altered splice site)
23732375TURNmight get lost (downstream of altered splice site)
23762378STRANDmight get lost (downstream of altered splice site)
23802382TURNmight get lost (downstream of altered splice site)
23842386STRANDmight get lost (downstream of altered splice site)
23882393HELIXmight get lost (downstream of altered splice site)
23992406HELIXmight get lost (downstream of altered splice site)
24062440REPEATPlectin 11.might get lost (downstream of altered splice site)
24142417STRANDmight get lost (downstream of altered splice site)
24182421TURNmight get lost (downstream of altered splice site)
24222424STRANDmight get lost (downstream of altered splice site)
24262431HELIXmight get lost (downstream of altered splice site)
24372439TURNmight get lost (downstream of altered splice site)
24422446STRANDmight get lost (downstream of altered splice site)
24562493REPEATPlectin 12.might get lost (downstream of altered splice site)
24802480LIPIDOmega-hydroxyceramide glutamate ester (Potential).might get lost (downstream of altered splice site)
25072544REPEATPlectin 13.might get lost (downstream of altered splice site)
26062606MOD_RESPhosphoserine.might get lost (downstream of altered splice site)
26092822REGION4.5 X 38 AA tandem repeats (Domain C).might get lost (downstream of altered splice site)
26102647REPEATPlectin 14.might get lost (downstream of altered splice site)
26192624STRANDmight get lost (downstream of altered splice site)
26252628TURNmight get lost (downstream of altered splice site)
26292631STRANDmight get lost (downstream of altered splice site)
26332638HELIXmight get lost (downstream of altered splice site)
26442655HELIXmight get lost (downstream of altered splice site)
26482685REPEATPlectin 15.might get lost (downstream of altered splice site)
26562658TURNmight get lost (downstream of altered splice site)
26592661STRANDmight get lost (downstream of altered splice site)
26632665TURNmight get lost (downstream of altered splice site)
26712676HELIXmight get lost (downstream of altered splice site)
26822696HELIXmight get lost (downstream of altered splice site)
26872688CONFLICTRL -> SV (in Ref. 1; AAA85135 and 4; AAA35766).might get lost (downstream of altered splice site)
27092714HELIXmight get lost (downstream of altered splice site)
27202732HELIXmight get lost (downstream of altered splice site)
27242761REPEATPlectin 16.might get lost (downstream of altered splice site)
27392741HELIXmight get lost (downstream of altered splice site)
27472752HELIXmight get lost (downstream of altered splice site)
27582765HELIXmight get lost (downstream of altered splice site)
27622799REPEATPlectin 17.might get lost (downstream of altered splice site)
27672769HELIXmight get lost (downstream of altered splice site)
27772779TURNmight get lost (downstream of altered splice site)
27852791HELIXmight get lost (downstream of altered splice site)
27962798TURNmight get lost (downstream of altered splice site)
28012805STRANDmight get lost (downstream of altered splice site)
28152815MOD_RESPhosphoserine.might get lost (downstream of altered splice site)
28202820MOD_RESPhosphoserine.might get lost (downstream of altered splice site)
28212821MOD_RESPhosphoserine.might get lost (downstream of altered splice site)
28242847REGION6 X 4 AA tandem repeats of G-S-R-[SR].might get lost (downstream of altered splice site)
28252825MOD_RESPhosphoserine.might get lost (downstream of altered splice site)
28492849MOD_RESPhosphoserine.might get lost (downstream of altered splice site)
28492849MUTAGENS->G: Increases association with KRT5- KRT14, KRT8-KRT18 or VIM intermediate filaments.might get lost (downstream of altered splice site)
28532853MOD_RESPhosphothreonine.might get lost (downstream of altered splice site)
28572857MOD_RESPhosphoserine.might get lost (downstream of altered splice site)
28682868MOD_RESPhosphoserine.might get lost (downstream of altered splice site)
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 8616 / 8616
position (AA) of stopcodon in wt / mu AA sequence 2872 / 2872
position of stopcodon in wt / mu cDNA 8957 / 8957
poly(A) signal N/A
conservation
nucleotide level for all changes - no scoring up to now
N/A
position of start ATG in wt / mu cDNA 342 / 342
chromosome 6
strand 1
last intron/exon boundary 5721
theoretical NMD boundary in CDS 5329
length of CDS 8616
coding sequence (CDS) position 88
cDNA position
(for ins/del: last normal base / first normal base)
429
gDNA position
(for ins/del: last normal base / first normal base)
429
chromosomal position
(for ins/del: last normal base / first normal base)
7542236
original gDNA sequence snippet GCCCGGACCTGCGCTACGAGGTGACCAGCGGCGGCGGGGGC
altered gDNA sequence snippet GCCCGGACCTGCGCTACGAGATGACCAGCGGCGGCGGGGGC
original cDNA sequence snippet GCCCGGACCTGCGCTACGAGGTGACCAGCGGCGGCGGGGGC
altered cDNA sequence snippet GCCCGGACCTGCGCTACGAGATGACCAGCGGCGGCGGGGGC
wildtype AA sequence MSCNGGSHPR INTLGRMIRA ESGPDLRYEV TSGGGGTSRM YYSRRGVITD QNSDGYCQTG
TMSRHQNQNT IQELLQNCSD CLMRAELIVQ PELKYGDGIQ LTRSRELDEC FAQANDQMEI
LDSLIREMRQ MGQPCDAYQK RLLQLQEQMR ALYKAISVPR VRRASSKGGG GYTCQSGSGW
DEFTKHVTSE CLGWMRQQRA EMDMVAWGVD LASVEQHINS HRGIHNSIGD YRWQLDKIKA
DLREKSAIYQ LEEEYENLLK ASFERMDHLR QLQNIIQATS REIMWINDCE EEELLYDWSD
KNTNIAQKQE AFSIRMSQLE VKEKELNKLK QESDQLVLNQ HPASDKIEAY MDTLQTQWSW
ILQITKCIDV HLKENAAYFQ FFEEAQSTEA YLKGLQDSIR KKYPCDKNMP LQHLLEQIKE
LEKEREKILE YKRQVQNLVN KSKKIVQLKP RNPDYRSNKP IILRALCDYK QDQKIVHKGD
ECILKDNNER SKWYVTGPGG VDMLVPSVGL IIPPPNPLAV DLSCKIEQYY EAILALWNQL
YINMKSLVSW HYCMIDIEKI RAMTIAKLKT MRQEDYMKTI ADLELHYQEF IRNSQGSEMF
GDDDKRKIQS QFTDAQKHYQ TLVIQLPGYP QHQTVTTTEI THHGTCQDVN HNKVIETNRE
NDKQETWMLM ELQKIRRQIE HCEGRMTLKN LPLADQGSSH HITVKINELK SVQNDSQAIA
EVLNQLKDML ANFRGSEKYC YLQNEVFGLF QKLENINGVT DGYLNSLCTV RALLQAILQT
EDMLKVYEAR LTEEETVCLD LDKVEAYRCG LKKIKNDLNL KKSLLATMKT ELQKAQQIHS
QTSQQYPLYD LDLGKFGEKV TQLTDRWQRI DKQIDFRLWD LEKQIKQLRN YRDNYQAFCK
WLYDAKRRQD SLESMKFGDS NTVMRFLNEQ KNLHSEISGK RDKSEEVQKI AELCANSIKD
YELQLASYTS GLETLLNIPI KRTMIQSPSG VILQEAADVH ARYIELLTRS GDYYRFLSEM
LKSLEDLKLK NTKIEVLEEE LRLARDANSE NCNKNKFLDQ NLQKYQAECS QFKAKLASLE
ELKRQAELDG KSAKQNLDKC YGQIKELNEK ITRLTYEIED EKRRRKSVED RFDQQKNDYD
QLQKARQCEK ENLGWQKLES EKAIKEKEYE IERLRVLLQE EGTRKREYEN ELAKVRNHYN
EEMSNLRNKY ETEINITKTT IKEISMQKED DSKNLRNQLD RLSRENRDLK DEIVRLNDSI
LQATEQRRRA EENALQQKAC GSEIMQKKQH LEIELKQVMQ QRSEDNARHK QSLEEAAKTI
QDKNKEIERL KAEFQEEAKR RWEYENELSK VRNNYDEEII SLKNQFETEI NITKTTIHQL
TMQKEEDTSG YRAQIDNLTR ENRSLSEEIK RLKNTLTQTT ENLRRVEEDI QQQKATGSEV
SQRKQQLEVE LRQVTQMRTE ESVRYKQSLD DAAKTIQDKN KEIERLKQLI DKETNDRKCL
EDENARLQRV QYDLQKANSS ATETINKLKV QEQELTRLRI DYERVSQERT VKDQDITRFQ
NSLKELQLQK QKVEEELNRL KRTASEDSCK RKKLEEELEG MRRSLKEQAI KITNLTQQLE
QASIVKKRSE DDLRQQRDVL DGHLREKQRT QEELRRLSSE VEALRRQLLQ EQESVKQAHL
RNEHFQKAIE DKSRSLNESK IEIERLQSLT ENLTKEHLML EEELRNLRLE YDDLRRGRSE
ADSDKNATIL ELRSQLQISN NRTLELQGLI NDLQRERENL RQEIEKFQKQ ALEASNRIQE
SKNQCTQVVQ ERESLLVKIK VLEQDKARLQ RLEDELNRAK STLEAETRVK QRLECEKQQI
QNDLNQWKTQ YSRKEEAIRK IESEREKSER EKNSLRSEIE RLQAEIKRIE ERCRRKLEDS
TRETQSQLET ERSRYQREID KLRQRPYGSH RETQTECEWT VDTSKLVFDG LRKKVTAMQL
YECQLIDKTT LDKLLKGKKS VEEVASEIQP FLRGAGSIAG ASASPKEKYS LVEAKRKKLI
SPESTVMLLE AQAATGGIID PHRNEKLTVD SAIARDLIDF DDRQQIYAAE KAITGFDDPF
SGKTVSVSEA IKKNLIDRET GMRLLEAQIA SGGVVDPVNS VFLPKDVALA RGLIDRDLYR
SLNDPRDSQK NFVDPVTKKK VSYVQLKERC RIEPHTGLLL LSVQKRSMSF QGIRQPVTVT
ELVDSGILRP STVNELESGQ ISYDEVGERI KDFLQGSSCI AGIYNETTKQ KLGIYEAMKI
GLVRPGTALE LLEAQAATGF IVDPVSNLRL PVEEAYKRGL VGIEFKEKLL SAERAVTGYN
DPETGNIISL FQAMNKELIE KGHGIRLLEA QIATGGIIDP KESHRLPVDI AYKRGYFNEE
LSEILSDPSD DTKGFFDPNT EENLTYLQLK ERCIKDEETG LCLLPLKEKK KQVQTSQKNT
LRKRRVVIVD PETNKEMSVQ EAYKKGLIDY ETFKELCEQE CEWEEITITG SDGSTRVVLV
DRKTGSQYDI QDAIDKGLVD RKFFDQYRSG SLSLTQFADM ISLKNGVGTS SSMGSGVSDD
VFSSSRHESV SKISTISSVR NLTIRSSSFS DTLEESSPIA AIFDTENLEK ISITEGIERG
IVDSITGQRL LEAQACTGGI IHPTTGQKLS LQDAVSQGVI DQDMATRLKP AQKAFIGFEG
VKGKKKMSAA EAVKEKWLPY EAGQRFLEFQ YLTGGLVDPE VHGRISTEEA IRKGFIDGRA
AQRLQDTSSY AKILTCPKTK LKISYKDAIN RSMVEDITGL RLLEAASVSS KGLPSPYNMS
SAPGSRSGSR SGSRSGSRSG SRSGSRRGSF DATGNSSYSY SYSFSSSSIG H*
mutated AA sequence MSCNGGSHPR INTLGRMIRA ESGPDLRYEM TSGGGGTSRM YYSRRGVITD QNSDGYCQTG
TMSRHQNQNT IQELLQNCSD CLMRAELIVQ PELKYGDGIQ LTRSRELDEC FAQANDQMEI
LDSLIREMRQ MGQPCDAYQK RLLQLQEQMR ALYKAISVPR VRRASSKGGG GYTCQSGSGW
DEFTKHVTSE CLGWMRQQRA EMDMVAWGVD LASVEQHINS HRGIHNSIGD YRWQLDKIKA
DLREKSAIYQ LEEEYENLLK ASFERMDHLR QLQNIIQATS REIMWINDCE EEELLYDWSD
KNTNIAQKQE AFSIRMSQLE VKEKELNKLK QESDQLVLNQ HPASDKIEAY MDTLQTQWSW
ILQITKCIDV HLKENAAYFQ FFEEAQSTEA YLKGLQDSIR KKYPCDKNMP LQHLLEQIKE
LEKEREKILE YKRQVQNLVN KSKKIVQLKP RNPDYRSNKP IILRALCDYK QDQKIVHKGD
ECILKDNNER SKWYVTGPGG VDMLVPSVGL IIPPPNPLAV DLSCKIEQYY EAILALWNQL
YINMKSLVSW HYCMIDIEKI RAMTIAKLKT MRQEDYMKTI ADLELHYQEF IRNSQGSEMF
GDDDKRKIQS QFTDAQKHYQ TLVIQLPGYP QHQTVTTTEI THHGTCQDVN HNKVIETNRE
NDKQETWMLM ELQKIRRQIE HCEGRMTLKN LPLADQGSSH HITVKINELK SVQNDSQAIA
EVLNQLKDML ANFRGSEKYC YLQNEVFGLF QKLENINGVT DGYLNSLCTV RALLQAILQT
EDMLKVYEAR LTEEETVCLD LDKVEAYRCG LKKIKNDLNL KKSLLATMKT ELQKAQQIHS
QTSQQYPLYD LDLGKFGEKV TQLTDRWQRI DKQIDFRLWD LEKQIKQLRN YRDNYQAFCK
WLYDAKRRQD SLESMKFGDS NTVMRFLNEQ KNLHSEISGK RDKSEEVQKI AELCANSIKD
YELQLASYTS GLETLLNIPI KRTMIQSPSG VILQEAADVH ARYIELLTRS GDYYRFLSEM
LKSLEDLKLK NTKIEVLEEE LRLARDANSE NCNKNKFLDQ NLQKYQAECS QFKAKLASLE
ELKRQAELDG KSAKQNLDKC YGQIKELNEK ITRLTYEIED EKRRRKSVED RFDQQKNDYD
QLQKARQCEK ENLGWQKLES EKAIKEKEYE IERLRVLLQE EGTRKREYEN ELAKVRNHYN
EEMSNLRNKY ETEINITKTT IKEISMQKED DSKNLRNQLD RLSRENRDLK DEIVRLNDSI
LQATEQRRRA EENALQQKAC GSEIMQKKQH LEIELKQVMQ QRSEDNARHK QSLEEAAKTI
QDKNKEIERL KAEFQEEAKR RWEYENELSK VRNNYDEEII SLKNQFETEI NITKTTIHQL
TMQKEEDTSG YRAQIDNLTR ENRSLSEEIK RLKNTLTQTT ENLRRVEEDI QQQKATGSEV
SQRKQQLEVE LRQVTQMRTE ESVRYKQSLD DAAKTIQDKN KEIERLKQLI DKETNDRKCL
EDENARLQRV QYDLQKANSS ATETINKLKV QEQELTRLRI DYERVSQERT VKDQDITRFQ
NSLKELQLQK QKVEEELNRL KRTASEDSCK RKKLEEELEG MRRSLKEQAI KITNLTQQLE
QASIVKKRSE DDLRQQRDVL DGHLREKQRT QEELRRLSSE VEALRRQLLQ EQESVKQAHL
RNEHFQKAIE DKSRSLNESK IEIERLQSLT ENLTKEHLML EEELRNLRLE YDDLRRGRSE
ADSDKNATIL ELRSQLQISN NRTLELQGLI NDLQRERENL RQEIEKFQKQ ALEASNRIQE
SKNQCTQVVQ ERESLLVKIK VLEQDKARLQ RLEDELNRAK STLEAETRVK QRLECEKQQI
QNDLNQWKTQ YSRKEEAIRK IESEREKSER EKNSLRSEIE RLQAEIKRIE ERCRRKLEDS
TRETQSQLET ERSRYQREID KLRQRPYGSH RETQTECEWT VDTSKLVFDG LRKKVTAMQL
YECQLIDKTT LDKLLKGKKS VEEVASEIQP FLRGAGSIAG ASASPKEKYS LVEAKRKKLI
SPESTVMLLE AQAATGGIID PHRNEKLTVD SAIARDLIDF DDRQQIYAAE KAITGFDDPF
SGKTVSVSEA IKKNLIDRET GMRLLEAQIA SGGVVDPVNS VFLPKDVALA RGLIDRDLYR
SLNDPRDSQK NFVDPVTKKK VSYVQLKERC RIEPHTGLLL LSVQKRSMSF QGIRQPVTVT
ELVDSGILRP STVNELESGQ ISYDEVGERI KDFLQGSSCI AGIYNETTKQ KLGIYEAMKI
GLVRPGTALE LLEAQAATGF IVDPVSNLRL PVEEAYKRGL VGIEFKEKLL SAERAVTGYN
DPETGNIISL FQAMNKELIE KGHGIRLLEA QIATGGIIDP KESHRLPVDI AYKRGYFNEE
LSEILSDPSD DTKGFFDPNT EENLTYLQLK ERCIKDEETG LCLLPLKEKK KQVQTSQKNT
LRKRRVVIVD PETNKEMSVQ EAYKKGLIDY ETFKELCEQE CEWEEITITG SDGSTRVVLV
DRKTGSQYDI QDAIDKGLVD RKFFDQYRSG SLSLTQFADM ISLKNGVGTS SSMGSGVSDD
VFSSSRHESV SKISTISSVR NLTIRSSSFS DTLEESSPIA AIFDTENLEK ISITEGIERG
IVDSITGQRL LEAQACTGGI IHPTTGQKLS LQDAVSQGVI DQDMATRLKP AQKAFIGFEG
VKGKKKMSAA EAVKEKWLPY EAGQRFLEFQ YLTGGLVDPE VHGRISTEEA IRKGFIDGRA
AQRLQDTSSY AKILTCPKTK LKISYKDAIN RSMVEDITGL RLLEAASVSS KGLPSPYNMS
SAPGSRSGSR SGSRSGSRSG SRSGSRRGSF DATGNSSYSY SYSFSSSSIG H*
speed 0.20 s
All positions are in basepairs (bp) if not explicitly stated differently.
AA/aa: amino acid; CDS: coding sequence; mu: mutated; NMD: nonsense-mediated mRNA decay; nt: nucleotide; wt: wildtype; TGP: 1000 Genomes Project
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Yum, tasty mutations...

mutation t@sting

documentation

Prediction

polymorphism

Model: simple_aae, prob: 0.999999748606928      (explain)
Summary
  • amino acid sequence changed
  • heterozygous in TGP or ExAC
  • known as potential disease variant: rs16846 (probable pathogenic)
  • known disease mutation at this position (HGMD CM063961)
  • protein features (might be) affected
  • splice site changes
hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr6:7542236G>AN/A show variant in all transcripts   IGV
HGNC symbol DSP
Ensembl transcript ID ENST00000418664
Genbank transcript ID NM_001008844
UniProt peptide P15924
alteration type single base exchange
alteration region CDS
DNA changes c.88G>A
cDNA.387G>A
g.429G>A
AA changes V30M Score: 21 explain score(s)
position(s) of altered AA
if AA alteration in CDS
30
frameshift no
known variant Reference ID: rs121912998
databasehomozygous (A/A)heterozygousallele carriers
1000G01111
ExAC1147148

known as potential disease variant: rs16846 (probable pathogenic for Cardiomyopathy|Right ventricular cardiomyopathy|Dilated cardiomyopathy with woolly hair and keratoderma|Arrhythmogenic right ventricular dysplasia 8|Skin fragility-woolly hair-palmoplantar keratoderma syndrome|Lethal acantholytic epidermolysis bullosa|Keratosis palmoplantaris striata II|Arrhythmogenic right ventricular cardiomyopathy|not specified|Cardiovascular phenotype|not provided) dbSNP  NCBI variation viewer
known disease mutation at this position, please check HGMD for details (HGMD ID CM063961)

known disease mutation at this position, please check HGMD for details (HGMD ID CM063961)
known disease mutation at this position, please check HGMD for details (HGMD ID CM063961)
regulatory features Promoter Associated, Regulatory Feature, Promoter like regulatory feature
H3K4me2, Histone, Histone 3 Lysine 4 Di-Methylation
H3K27me3, Histone, Histone 3 Lysine 27 Tri-Methylation
PolII, Polymerase, RNA Polymerase II
H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
H2AZ, Histone, Histone 2A variant Z
HEY1, Transcription Factor, HEY1 Transcription Factor Binding
H3K9ac, Histone, Histone 3 Lysine 9 Acetylation
H3K27ac, Histone, Histone 3 Lysine 27 Acetylation
TAF1, Transcription Factor, TAF1 Transcription Factor Binding
H3K4me3, Histone, Histone 3 Lysine 4 Tri-Methylation
DNase1, Open Chromatin, DNase1 Hypersensitive Site
phyloP / phastCons
PhyloPPhastCons
(flanking)1.3470.905
-2.50.304
(flanking)0.4260.518
explain score(s) and/or inspect your position(s) in in UCSC Genome Browser
splice sites
effectgDNA positionscorewt detection sequence exon-intron border
Donor increased425wt: 0.84 / mu: 0.99wt: CGCTACGAGGTGACC
mu: CGCTACGAGATGACC
 CTAC|gagg
Donor increased427wt: 0.45 / mu: 0.59wt: CTACGAGGTGACCAG
mu: CTACGAGATGACCAG
 ACGA|ggtg
Donor gained4300.32mu: CGAGATGACCAGCGG AGAT|gacc
distance from splice site 83
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      30RAESGPDLRYEVTSGGGGTSRMYY
mutated  all conserved    30RAESGPDLRYEMTSGGGGTSRMY
Ptroglodytes  all identical  ENSPTRG00000017702  30RAESGPDLRYEVTSGGGGTSRMY
Mmulatta  all conserved  ENSMMUG00000014784  30RAESGPDLRYEMTSGGGGTSRIY
Fcatus  no homologue    
Mmusculus  all conserved  ENSMUSG00000054889  30RAESGPDLRYEMTYSGGGGGGGGGGGGGTSRTF
Ggallus  all conserved  ENSGALG00000012790  30RADSGTDLRYEMSSHVVGGGGGGTHTHKTY
Trubripes  no homologue    
Drerio  no alignment  ENSDARG00000022309  n/a
Dmelanogaster  no homologue    
Celegans  no homologue    
Xtropicalis  no homologue    
protein features
start (aa)end (aa)featuredetails 
1584REGIONInteracts with plakophilin 1 and junction plakoglobin.lost
11056REGIONGlobular 1.lost
2828MOD_RESPhosphotyrosine.might get lost (downstream of altered splice site)
5656MOD_RESPhosphotyrosine.might get lost (downstream of altered splice site)
165165MOD_RESPhosphoserine.might get lost (downstream of altered splice site)
166166MOD_RESPhosphoserine.might get lost (downstream of altered splice site)
176176MOD_RESPhosphoserine.might get lost (downstream of altered splice site)
178178MOD_RESPhosphoserine.might get lost (downstream of altered splice site)
178271REPEATSpectrin 1.might get lost (downstream of altered splice site)
182201HELIXmight get lost (downstream of altered splice site)
211241HELIXmight get lost (downstream of altered splice site)
245294HELIXmight get lost (downstream of altered splice site)
272375REPEATSpectrin 2.might get lost (downstream of altered splice site)
307338HELIXmight get lost (downstream of altered splice site)
344402HELIXmight get lost (downstream of altered splice site)
376446REPEATSpectrin 3a.might get lost (downstream of altered splice site)
411442HELIXmight get lost (downstream of altered splice site)
447515DOMAINSH3.might get lost (downstream of altered splice site)
449451HELIXmight get lost (downstream of altered splice site)
462467STRANDmight get lost (downstream of altered splice site)
469471STRANDmight get lost (downstream of altered splice site)
474476STRANDmight get lost (downstream of altered splice site)
481486STRANDmight get lost (downstream of altered splice site)
488496STRANDmight get lost (downstream of altered splice site)
498500STRANDmight get lost (downstream of altered splice site)
503506STRANDmight get lost (downstream of altered splice site)
507509HELIXmight get lost (downstream of altered splice site)
516545REPEATSpectrin 3b.might get lost (downstream of altered splice site)
517561HELIXmight get lost (downstream of altered splice site)
546627REPEATSpectrin 4.might get lost (downstream of altered splice site)
565568HELIXmight get lost (downstream of altered splice site)
573575TURNmight get lost (downstream of altered splice site)
576594HELIXmight get lost (downstream of altered splice site)
602624HELIXmight get lost (downstream of altered splice site)
654769REPEATSpectrin 5.might get lost (downstream of altered splice site)
770883REPEATSpectrin 6.might get lost (downstream of altered splice site)
905905CONFLICTA -> R (in Ref. 1; AAA85135).might get lost (downstream of altered splice site)
10181945COILEDPotential.might get lost (downstream of altered splice site)
10571945REGIONCentral fibrous rod domain.might get lost (downstream of altered splice site)
11201120CONFLICTD -> R (in Ref. 4; AAA35766).might get lost (downstream of altered splice site)
12201220MOD_RESPhosphothreonine.might get lost (downstream of altered splice site)
12251225MOD_RESPhosphoserine.might get lost (downstream of altered splice site)
19462871REGIONGlobular 2.might get lost (downstream of altered splice site)
19602208REGION4.5 X 38 AA tandem repeats (Domain A).might get lost (downstream of altered splice site)
20092045REPEATPlectin 1.might get lost (downstream of altered splice site)
20242024MOD_RESPhosphoserine.might get lost (downstream of altered splice site)
20462083REPEATPlectin 2.might get lost (downstream of altered splice site)
20842121REPEATPlectin 3.might get lost (downstream of altered splice site)
21222159REPEATPlectin 4.might get lost (downstream of altered splice site)
21632197REPEATPlectin 5.might get lost (downstream of altered splice site)
21982233REPEATPlectin 6.might get lost (downstream of altered splice site)
22092209MOD_RESPhosphoserine.might get lost (downstream of altered splice site)
22132217STRANDmight get lost (downstream of altered splice site)
22192224HELIXmight get lost (downstream of altered splice site)
22302237HELIXmight get lost (downstream of altered splice site)
22442446REGION4.5 X 38 AA tandem repeats (Domain B).might get lost (downstream of altered splice site)
22462249HELIXmight get lost (downstream of altered splice site)
22512254HELIXmight get lost (downstream of altered splice site)
22512288REPEATPlectin 7.might get lost (downstream of altered splice site)
22602265STRANDmight get lost (downstream of altered splice site)
22662269TURNmight get lost (downstream of altered splice site)
22702273STRANDmight get lost (downstream of altered splice site)
22742278HELIXmight get lost (downstream of altered splice site)
22752275MOD_RESPhosphotyrosine.might get lost (downstream of altered splice site)
22792283STRANDmight get lost (downstream of altered splice site)
22852296HELIXmight get lost (downstream of altered splice site)
22892326REPEATPlectin 8.might get lost (downstream of altered splice site)
23012303STRANDmight get lost (downstream of altered splice site)
23042307TURNmight get lost (downstream of altered splice site)
23082310STRANDmight get lost (downstream of altered splice site)
23122317HELIXmight get lost (downstream of altered splice site)
23232333TURNmight get lost (downstream of altered splice site)
23272364REPEATPlectin 9.might get lost (downstream of altered splice site)
23342337HELIXmight get lost (downstream of altered splice site)
23422344TURNmight get lost (downstream of altered splice site)
23502354HELIXmight get lost (downstream of altered splice site)
23552357TURNmight get lost (downstream of altered splice site)
23612372HELIXmight get lost (downstream of altered splice site)
23652402REPEATPlectin 10.might get lost (downstream of altered splice site)
23732375TURNmight get lost (downstream of altered splice site)
23762378STRANDmight get lost (downstream of altered splice site)
23802382TURNmight get lost (downstream of altered splice site)
23842386STRANDmight get lost (downstream of altered splice site)
23882393HELIXmight get lost (downstream of altered splice site)
23992406HELIXmight get lost (downstream of altered splice site)
24062440REPEATPlectin 11.might get lost (downstream of altered splice site)
24142417STRANDmight get lost (downstream of altered splice site)
24182421TURNmight get lost (downstream of altered splice site)
24222424STRANDmight get lost (downstream of altered splice site)
24262431HELIXmight get lost (downstream of altered splice site)
24372439TURNmight get lost (downstream of altered splice site)
24422446STRANDmight get lost (downstream of altered splice site)
24562493REPEATPlectin 12.might get lost (downstream of altered splice site)
24802480LIPIDOmega-hydroxyceramide glutamate ester (Potential).might get lost (downstream of altered splice site)
25072544REPEATPlectin 13.might get lost (downstream of altered splice site)
26062606MOD_RESPhosphoserine.might get lost (downstream of altered splice site)
26092822REGION4.5 X 38 AA tandem repeats (Domain C).might get lost (downstream of altered splice site)
26102647REPEATPlectin 14.might get lost (downstream of altered splice site)
26192624STRANDmight get lost (downstream of altered splice site)
26252628TURNmight get lost (downstream of altered splice site)
26292631STRANDmight get lost (downstream of altered splice site)
26332638HELIXmight get lost (downstream of altered splice site)
26442655HELIXmight get lost (downstream of altered splice site)
26482685REPEATPlectin 15.might get lost (downstream of altered splice site)
26562658TURNmight get lost (downstream of altered splice site)
26592661STRANDmight get lost (downstream of altered splice site)
26632665TURNmight get lost (downstream of altered splice site)
26712676HELIXmight get lost (downstream of altered splice site)
26822696HELIXmight get lost (downstream of altered splice site)
26872688CONFLICTRL -> SV (in Ref. 1; AAA85135 and 4; AAA35766).might get lost (downstream of altered splice site)
27092714HELIXmight get lost (downstream of altered splice site)
27202732HELIXmight get lost (downstream of altered splice site)
27242761REPEATPlectin 16.might get lost (downstream of altered splice site)
27392741HELIXmight get lost (downstream of altered splice site)
27472752HELIXmight get lost (downstream of altered splice site)
27582765HELIXmight get lost (downstream of altered splice site)
27622799REPEATPlectin 17.might get lost (downstream of altered splice site)
27672769HELIXmight get lost (downstream of altered splice site)
27772779TURNmight get lost (downstream of altered splice site)
27852791HELIXmight get lost (downstream of altered splice site)
27962798TURNmight get lost (downstream of altered splice site)
28012805STRANDmight get lost (downstream of altered splice site)
28152815MOD_RESPhosphoserine.might get lost (downstream of altered splice site)
28202820MOD_RESPhosphoserine.might get lost (downstream of altered splice site)
28212821MOD_RESPhosphoserine.might get lost (downstream of altered splice site)
28242847REGION6 X 4 AA tandem repeats of G-S-R-[SR].might get lost (downstream of altered splice site)
28252825MOD_RESPhosphoserine.might get lost (downstream of altered splice site)
28492849MOD_RESPhosphoserine.might get lost (downstream of altered splice site)
28492849MUTAGENS->G: Increases association with KRT5- KRT14, KRT8-KRT18 or VIM intermediate filaments.might get lost (downstream of altered splice site)
28532853MOD_RESPhosphothreonine.might get lost (downstream of altered splice site)
28572857MOD_RESPhosphoserine.might get lost (downstream of altered splice site)
28682868MOD_RESPhosphoserine.might get lost (downstream of altered splice site)
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 6819 / 6819
position (AA) of stopcodon in wt / mu AA sequence 2273 / 2273
position of stopcodon in wt / mu cDNA 7118 / 7118
poly(A) signal N/A
conservation
nucleotide level for all changes - no scoring up to now
N/A
position of start ATG in wt / mu cDNA 300 / 300
chromosome 6
strand 1
last intron/exon boundary 3882
theoretical NMD boundary in CDS 3532
length of CDS 6819
coding sequence (CDS) position 88
cDNA position
(for ins/del: last normal base / first normal base)
387
gDNA position
(for ins/del: last normal base / first normal base)
429
chromosomal position
(for ins/del: last normal base / first normal base)
7542236
original gDNA sequence snippet GCCCGGACCTGCGCTACGAGGTGACCAGCGGCGGCGGGGGC
altered gDNA sequence snippet GCCCGGACCTGCGCTACGAGATGACCAGCGGCGGCGGGGGC
original cDNA sequence snippet GCCCGGACCTGCGCTACGAGGTGACCAGCGGCGGCGGGGGC
altered cDNA sequence snippet GCCCGGACCTGCGCTACGAGATGACCAGCGGCGGCGGGGGC
wildtype AA sequence MSCNGGSHPR INTLGRMIRA ESGPDLRYEV TSGGGGTSRM YYSRRGVITD QNSDGYCQTG
TMSRHQNQNT IQELLQNCSD CLMRAELIVQ PELKYGDGIQ LTRSRELDEC FAQANDQMEI
LDSLIREMRQ MGQPCDAYQK RLLQLQEQMR ALYKAISVPR VRRASSKGGG GYTCQSGSGW
DEFTKHVTSE CLGWMRQQRA EMDMVAWGVD LASVEQHINS HRGIHNSIGD YRWQLDKIKA
DLREKSAIYQ LEEEYENLLK ASFERMDHLR QLQNIIQATS REIMWINDCE EEELLYDWSD
KNTNIAQKQE AFSIRMSQLE VKEKELNKLK QESDQLVLNQ HPASDKIEAY MDTLQTQWSW
ILQITKCIDV HLKENAAYFQ FFEEAQSTEA YLKGLQDSIR KKYPCDKNMP LQHLLEQIKE
LEKEREKILE YKRQVQNLVN KSKKIVQLKP RNPDYRSNKP IILRALCDYK QDQKIVHKGD
ECILKDNNER SKWYVTGPGG VDMLVPSVGL IIPPPNPLAV DLSCKIEQYY EAILALWNQL
YINMKSLVSW HYCMIDIEKI RAMTIAKLKT MRQEDYMKTI ADLELHYQEF IRNSQGSEMF
GDDDKRKIQS QFTDAQKHYQ TLVIQLPGYP QHQTVTTTEI THHGTCQDVN HNKVIETNRE
NDKQETWMLM ELQKIRRQIE HCEGRMTLKN LPLADQGSSH HITVKINELK SVQNDSQAIA
EVLNQLKDML ANFRGSEKYC YLQNEVFGLF QKLENINGVT DGYLNSLCTV RALLQAILQT
EDMLKVYEAR LTEEETVCLD LDKVEAYRCG LKKIKNDLNL KKSLLATMKT ELQKAQQIHS
QTSQQYPLYD LDLGKFGEKV TQLTDRWQRI DKQIDFRLWD LEKQIKQLRN YRDNYQAFCK
WLYDAKRRQD SLESMKFGDS NTVMRFLNEQ KNLHSEISGK RDKSEEVQKI AELCANSIKD
YELQLASYTS GLETLLNIPI KRTMIQSPSG VILQEAADVH ARYIELLTRS GDYYRFLSEM
LKSLEDLKLK NTKIEVLEEE LRLARDANSE NCNKNKFLDQ NLQKYQAECS QFKAKLASLE
ELKRQAELDG KSAKQNLDKC YGQIKELNEK ITRLTYEIED EKRRRKSVED RFDQQKNDYD
QLQKARQCEK ENLGWQKLES EKAIKEKEYE IERLRVLLQE EGTRKREYEN ELAKASNRIQ
ESKNQCTQVV QERESLLVKI KVLEQDKARL QRLEDELNRA KSTLEAETRV KQRLECEKQQ
IQNDLNQWKT QYSRKEEAIR KIESEREKSE REKNSLRSEI ERLQAEIKRI EERCRRKLED
STRETQSQLE TERSRYQREI DKLRQRPYGS HRETQTECEW TVDTSKLVFD GLRKKVTAMQ
LYECQLIDKT TLDKLLKGKK SVEEVASEIQ PFLRGAGSIA GASASPKEKY SLVEAKRKKL
ISPESTVMLL EAQAATGGII DPHRNEKLTV DSAIARDLID FDDRQQIYAA EKAITGFDDP
FSGKTVSVSE AIKKNLIDRE TGMRLLEAQI ASGGVVDPVN SVFLPKDVAL ARGLIDRDLY
RSLNDPRDSQ KNFVDPVTKK KVSYVQLKER CRIEPHTGLL LLSVQKRSMS FQGIRQPVTV
TELVDSGILR PSTVNELESG QISYDEVGER IKDFLQGSSC IAGIYNETTK QKLGIYEAMK
IGLVRPGTAL ELLEAQAATG FIVDPVSNLR LPVEEAYKRG LVGIEFKEKL LSAERAVTGY
NDPETGNIIS LFQAMNKELI EKGHGIRLLE AQIATGGIID PKESHRLPVD IAYKRGYFNE
ELSEILSDPS DDTKGFFDPN TEENLTYLQL KERCIKDEET GLCLLPLKEK KKQVQTSQKN
TLRKRRVVIV DPETNKEMSV QEAYKKGLID YETFKELCEQ ECEWEEITIT GSDGSTRVVL
VDRKTGSQYD IQDAIDKGLV DRKFFDQYRS GSLSLTQFAD MISLKNGVGT SSSMGSGVSD
DVFSSSRHES VSKISTISSV RNLTIRSSSF SDTLEESSPI AAIFDTENLE KISITEGIER
GIVDSITGQR LLEAQACTGG IIHPTTGQKL SLQDAVSQGV IDQDMATRLK PAQKAFIGFE
GVKGKKKMSA AEAVKEKWLP YEAGQRFLEF QYLTGGLVDP EVHGRISTEE AIRKGFIDGR
AAQRLQDTSS YAKILTCPKT KLKISYKDAI NRSMVEDITG LRLLEAASVS SKGLPSPYNM
SSAPGSRSGS RSGSRSGSRS GSRSGSRRGS FDATGNSSYS YSYSFSSSSI GH*
mutated AA sequence MSCNGGSHPR INTLGRMIRA ESGPDLRYEM TSGGGGTSRM YYSRRGVITD QNSDGYCQTG
TMSRHQNQNT IQELLQNCSD CLMRAELIVQ PELKYGDGIQ LTRSRELDEC FAQANDQMEI
LDSLIREMRQ MGQPCDAYQK RLLQLQEQMR ALYKAISVPR VRRASSKGGG GYTCQSGSGW
DEFTKHVTSE CLGWMRQQRA EMDMVAWGVD LASVEQHINS HRGIHNSIGD YRWQLDKIKA
DLREKSAIYQ LEEEYENLLK ASFERMDHLR QLQNIIQATS REIMWINDCE EEELLYDWSD
KNTNIAQKQE AFSIRMSQLE VKEKELNKLK QESDQLVLNQ HPASDKIEAY MDTLQTQWSW
ILQITKCIDV HLKENAAYFQ FFEEAQSTEA YLKGLQDSIR KKYPCDKNMP LQHLLEQIKE
LEKEREKILE YKRQVQNLVN KSKKIVQLKP RNPDYRSNKP IILRALCDYK QDQKIVHKGD
ECILKDNNER SKWYVTGPGG VDMLVPSVGL IIPPPNPLAV DLSCKIEQYY EAILALWNQL
YINMKSLVSW HYCMIDIEKI RAMTIAKLKT MRQEDYMKTI ADLELHYQEF IRNSQGSEMF
GDDDKRKIQS QFTDAQKHYQ TLVIQLPGYP QHQTVTTTEI THHGTCQDVN HNKVIETNRE
NDKQETWMLM ELQKIRRQIE HCEGRMTLKN LPLADQGSSH HITVKINELK SVQNDSQAIA
EVLNQLKDML ANFRGSEKYC YLQNEVFGLF QKLENINGVT DGYLNSLCTV RALLQAILQT
EDMLKVYEAR LTEEETVCLD LDKVEAYRCG LKKIKNDLNL KKSLLATMKT ELQKAQQIHS
QTSQQYPLYD LDLGKFGEKV TQLTDRWQRI DKQIDFRLWD LEKQIKQLRN YRDNYQAFCK
WLYDAKRRQD SLESMKFGDS NTVMRFLNEQ KNLHSEISGK RDKSEEVQKI AELCANSIKD
YELQLASYTS GLETLLNIPI KRTMIQSPSG VILQEAADVH ARYIELLTRS GDYYRFLSEM
LKSLEDLKLK NTKIEVLEEE LRLARDANSE NCNKNKFLDQ NLQKYQAECS QFKAKLASLE
ELKRQAELDG KSAKQNLDKC YGQIKELNEK ITRLTYEIED EKRRRKSVED RFDQQKNDYD
QLQKARQCEK ENLGWQKLES EKAIKEKEYE IERLRVLLQE EGTRKREYEN ELAKASNRIQ
ESKNQCTQVV QERESLLVKI KVLEQDKARL QRLEDELNRA KSTLEAETRV KQRLECEKQQ
IQNDLNQWKT QYSRKEEAIR KIESEREKSE REKNSLRSEI ERLQAEIKRI EERCRRKLED
STRETQSQLE TERSRYQREI DKLRQRPYGS HRETQTECEW TVDTSKLVFD GLRKKVTAMQ
LYECQLIDKT TLDKLLKGKK SVEEVASEIQ PFLRGAGSIA GASASPKEKY SLVEAKRKKL
ISPESTVMLL EAQAATGGII DPHRNEKLTV DSAIARDLID FDDRQQIYAA EKAITGFDDP
FSGKTVSVSE AIKKNLIDRE TGMRLLEAQI ASGGVVDPVN SVFLPKDVAL ARGLIDRDLY
RSLNDPRDSQ KNFVDPVTKK KVSYVQLKER CRIEPHTGLL LLSVQKRSMS FQGIRQPVTV
TELVDSGILR PSTVNELESG QISYDEVGER IKDFLQGSSC IAGIYNETTK QKLGIYEAMK
IGLVRPGTAL ELLEAQAATG FIVDPVSNLR LPVEEAYKRG LVGIEFKEKL LSAERAVTGY
NDPETGNIIS LFQAMNKELI EKGHGIRLLE AQIATGGIID PKESHRLPVD IAYKRGYFNE
ELSEILSDPS DDTKGFFDPN TEENLTYLQL KERCIKDEET GLCLLPLKEK KKQVQTSQKN
TLRKRRVVIV DPETNKEMSV QEAYKKGLID YETFKELCEQ ECEWEEITIT GSDGSTRVVL
VDRKTGSQYD IQDAIDKGLV DRKFFDQYRS GSLSLTQFAD MISLKNGVGT SSSMGSGVSD
DVFSSSRHES VSKISTISSV RNLTIRSSSF SDTLEESSPI AAIFDTENLE KISITEGIER
GIVDSITGQR LLEAQACTGG IIHPTTGQKL SLQDAVSQGV IDQDMATRLK PAQKAFIGFE
GVKGKKKMSA AEAVKEKWLP YEAGQRFLEF QYLTGGLVDP EVHGRISTEE AIRKGFIDGR
AAQRLQDTSS YAKILTCPKT KLKISYKDAI NRSMVEDITG LRLLEAASVS SKGLPSPYNM
SSAPGSRSGS RSGSRSGSRS GSRSGSRRGS FDATGNSSYS YSYSFSSSSI GH*
speed 0.19 s
All positions are in basepairs (bp) if not explicitly stated differently.
AA/aa: amino acid; CDS: coding sequence; mu: mutated; NMD: nonsense-mediated mRNA decay; nt: nucleotide; wt: wildtype; TGP: 1000 Genomes Project
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