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 3 transcript(s)...
Querying Taster for transcript #1: ENST00000370225
Querying Taster for transcript #2: ENST00000536513
Querying Taster for transcript #3: ENST00000535881
MT speed 0 s - this script 4.793599 s

Results

genesymbolpredictionprobabilitymodelprediction
problem		splicingClinVaramino acid changesvariant typedbSNP IDprotein lengthfile
ABCA4disease_causing_automatic0.999999740597172simple_aae0L297Fsingle base exchangers61751408show file
ABCA4disease_causing_automatic0.999999740597172simple_aae0L146Fsingle base exchangers61751408show file
ABCA4disease_causing_automatic0.999999843789528simple_aae0L2027Fsingle base exchangers61751408show file

Taster files

Yum, tasty mutations...

mutation t@sting

 documentation

Prediction

disease causing

 Model: simple_aae, prob: 0.999999740597172 (classification due to ClinVar, real probability is shown anyway)      (explain)
Summary
  • amino acid sequence changed
  • known disease mutation at this position (HGMD CM970018)
  • known disease mutation: rs7882 (pathogenic)
  • protein features (might be) affected
 hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr1:94471065G>AN/A show variant in all transcripts   IGV
HGNC symbol ABCA4
Ensembl transcript ID ENST00000536513
Genbank transcript ID N/A
UniProt peptide P78363
alteration type single base exchange
alteration region CDS
DNA changes c.889C>T
cDNA.982C>T
g.115624C>T
AA changes L297F Score: 22 explain score(s)
position(s) of altered AA
if AA alteration in CDS		 297
frameshift no
known variant Reference ID: rs61751408
databasehomozygous (A/A)heterozygousallele carriers
1000G011
ExAC02626

known disease mutation: rs7882 (pathogenic for Retinal dystrophy|Age-related macular degeneration 2|Stargardt disease 1|Retinitis pigmentosa 19|Cone-rod dystrophy 3|Stargardt disease|not provided) dbSNP  NCBI variation viewer
known disease mutation at this position, please check HGMD for details (HGMD ID CM970018)

known disease mutation at this position, please check HGMD for details (HGMD ID CM970018)
known disease mutation at this position, please check HGMD for details (HGMD ID CM970018)
regulatory features H3K27me3, Histone, Histone 3 Lysine 27 Tri-Methylation
H3K4me1, Histone, Histone 3 Lysine 4 Mono-Methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)5.2051
4.6041
(flanking)1.3411
explain score(s) and/or inspect your position(s) in in UCSC Genome Browser
splice sites no abrogation of potential splice sites
distance from splice site 69
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      297YCPQFDAIDELLTGREHLYLYARL
mutated  not conserved    297YCPQFDAIDELFTGR
Ptroglodytes  all identical  ENSPTRG00000023377  2027YCPQFDAIDELLTGRE
Mmulatta  all identical  ENSMMUG00000013858  1018MCPQHNILFHHLTVAEHILFYAQ
Fcatus  no homologue    
Mmusculus  all identical  ENSMUSG00000028125  2026YCPQFDAIDDLLTGRE
Ggallus  all identical  ENSGALG00000005752  2021YCPQFDALDDLLTGRE
Trubripes  no homologue    
Drerio  all identical  ENSDARG00000062661  2092YCPQFDAIDELLTGRE
Dmelanogaster  no homologue    
Celegans  no homologue    
Xtropicalis  all identical  ENSXETG00000008223  2102YCPQFDAIDDLLTGRE
protein features
start (aa)end (aa)featuredetails 
43646TOPO_DOMExtracellular.lost
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 1632 / 1632
position (AA) of stopcodon in wt / mu AA sequence 544 / 544
position of stopcodon in wt / mu cDNA 1725 / 1725
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 94 / 94
chromosome 1
strand -1
last intron/exon boundary 1720
theoretical NMD boundary in CDS 1576
length of CDS 1632
coding sequence (CDS) position 889
cDNA position
(for ins/del: last normal base / first normal base)		 982
gDNA position
(for ins/del: last normal base / first normal base)		 115624
chromosomal position
(for ins/del: last normal base / first normal base)		 94471065
original gDNA sequence snippet TTGATGCAATTGATGAGCTGCTCACAGGACGAGAACATCTT
altered gDNA sequence snippet TTGATGCAATTGATGAGCTGTTCACAGGACGAGAACATCTT
original cDNA sequence snippet TTGATGCAATTGATGAGCTGCTCACAGGACGAGAACATCTT
altered cDNA sequence snippet TTGATGCAATTGATGAGCTGTTCACAGGACGAGAACATCTT
wildtype AA sequence MMMNYSVSAG LVVGIFIGFQ KKAYTSPENL PALVALLLLY GWAVIPMMYP ASFLFDVPST
AYVALSCANL FIGINSSAIT FILELFENNR TLLRFNAVLR KLLIVFPHFC LGRGLIDLAL
SQAVTDVYAR FGEEHSANPF HWDLIGKNLF AMVVEGVVYF LLTLLVQRHF FLSQWIAEPT
KEPIVDEDDD VAEERQRIIT GGNKTDILRL HELTKIYPGT SSPAVDRLCV GVRPGECFGL
LGVNGAGKTT TFKMLTGDTT VTSGDATVAG KSILTNISEV HQNMGYCPQF DAIDELLTGR
EHLYLYARLR GVPAEEIEKV ANWSIKSLGL TVYADCLAGT YSGGNKRKLS TAIALIGCPP
LVLLDEPTTG MDPQARRMLW NVIVSIIREG RAVVLTSHSM EECEALCTRL AIMVKGAFRC
MGTIQHLKSK FGDGYIVTMK IKSPKDDLLP DLNPVEQFFQ GNFPGSVQRE RHYNMLQFQV
SSSSLARIFQ LLLSHKDSLL IEEYSVTQTT LDQVFVNFAK QQTESHDLPL HPRAAGASRQ
AQD*
mutated AA sequence MMMNYSVSAG LVVGIFIGFQ KKAYTSPENL PALVALLLLY GWAVIPMMYP ASFLFDVPST
AYVALSCANL FIGINSSAIT FILELFENNR TLLRFNAVLR KLLIVFPHFC LGRGLIDLAL
SQAVTDVYAR FGEEHSANPF HWDLIGKNLF AMVVEGVVYF LLTLLVQRHF FLSQWIAEPT
KEPIVDEDDD VAEERQRIIT GGNKTDILRL HELTKIYPGT SSPAVDRLCV GVRPGECFGL
LGVNGAGKTT TFKMLTGDTT VTSGDATVAG KSILTNISEV HQNMGYCPQF DAIDELFTGR
EHLYLYARLR GVPAEEIEKV ANWSIKSLGL TVYADCLAGT YSGGNKRKLS TAIALIGCPP
LVLLDEPTTG MDPQARRMLW NVIVSIIREG RAVVLTSHSM EECEALCTRL AIMVKGAFRC
MGTIQHLKSK FGDGYIVTMK IKSPKDDLLP DLNPVEQFFQ GNFPGSVQRE RHYNMLQFQV
SSSSLARIFQ LLLSHKDSLL IEEYSVTQTT LDQVFVNFAK QQTESHDLPL HPRAAGASRQ
AQD*
speed 0.97 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
back to results table
Yum, tasty mutations...

mutation t@sting

 documentation

Prediction

disease causing

 Model: simple_aae, prob: 0.999999740597172 (classification due to ClinVar, real probability is shown anyway)      (explain)
Summary
  • amino acid sequence changed
  • known disease mutation at this position (HGMD CM970018)
  • known disease mutation: rs7882 (pathogenic)
  • protein features (might be) affected
 hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr1:94471065G>AN/A show variant in all transcripts   IGV
HGNC symbol ABCA4
Ensembl transcript ID ENST00000535881
Genbank transcript ID N/A
UniProt peptide P78363
alteration type single base exchange
alteration region CDS
DNA changes c.436C>T
cDNA.661C>T
g.115624C>T
AA changes L146F Score: 22 explain score(s)
position(s) of altered AA
if AA alteration in CDS		 146
frameshift no
known variant Reference ID: rs61751408
databasehomozygous (A/A)heterozygousallele carriers
1000G011
ExAC02626

known disease mutation: rs7882 (pathogenic for Retinal dystrophy|Age-related macular degeneration 2|Stargardt disease 1|Retinitis pigmentosa 19|Cone-rod dystrophy 3|Stargardt disease|not provided) dbSNP  NCBI variation viewer
known disease mutation at this position, please check HGMD for details (HGMD ID CM970018)

known disease mutation at this position, please check HGMD for details (HGMD ID CM970018)
known disease mutation at this position, please check HGMD for details (HGMD ID CM970018)
regulatory features H3K27me3, Histone, Histone 3 Lysine 27 Tri-Methylation
H3K4me1, Histone, Histone 3 Lysine 4 Mono-Methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)5.2051
4.6041
(flanking)1.3411
explain score(s) and/or inspect your position(s) in in UCSC Genome Browser
splice sites no abrogation of potential splice sites
distance from splice site 69
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      146YCPQFDAIDELLTGREHLYLYARL
mutated  not conserved    146YCPQFDAIDELFTGREHLYLYAR
Ptroglodytes  all identical  ENSPTRG00000023377  2027YCPQFDAIDELLTGREHLYLYAR
Mmulatta  all identical  ENSMMUG00000013858  1018MCPQHNILFHHLTVAEHILFYAQ
Fcatus  no homologue    
Mmusculus  all identical  ENSMUSG00000028125  2026YCPQFDAIDDLLTGREHLYLYAR
Ggallus  all identical  ENSGALG00000005752  2021YCPQFDALDDLLTGREHLYLYAR
Trubripes  no homologue    
Drerio  all identical  ENSDARG00000062661  2092YCPQFDAIDELLTGREHLYLYAR
Dmelanogaster  no homologue    
Celegans  no homologue    
Xtropicalis  all identical  ENSXETG00000008223  2102YCPQFDAIDDLLTGREHLQLYGR
protein features
start (aa)end (aa)featuredetails 
43646TOPO_DOMExtracellular.lost
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 1179 / 1179
position (AA) of stopcodon in wt / mu AA sequence 393 / 393
position of stopcodon in wt / mu cDNA 1404 / 1404
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 226 / 226
chromosome 1
strand -1
last intron/exon boundary 1399
theoretical NMD boundary in CDS 1123
length of CDS 1179
coding sequence (CDS) position 436
cDNA position
(for ins/del: last normal base / first normal base)		 661
gDNA position
(for ins/del: last normal base / first normal base)		 115624
chromosomal position
(for ins/del: last normal base / first normal base)		 94471065
original gDNA sequence snippet TTGATGCAATTGATGAGCTGCTCACAGGACGAGAACATCTT
altered gDNA sequence snippet TTGATGCAATTGATGAGCTGTTCACAGGACGAGAACATCTT
original cDNA sequence snippet TTGATGCAATTGATGAGCTGCTCACAGGACGAGAACATCTT
altered cDNA sequence snippet TTGATGCAATTGATGAGCTGTTCACAGGACGAGAACATCTT
wildtype AA sequence MVVEGVVYFL LTLLVQRHFF LSQWIAEPTK EPIVDEDDDV AEERQRIITG GNKTDILRLH
ELTKIYPGTS SPAVDRLCVG VRPGECFGLL GVNGAGKTTT FKMLTGDTTV TSGDATVAGK
SILTNISEVH QNMGYCPQFD AIDELLTGRE HLYLYARLRG VPAEEIEKVA NWSIKSLGLT
VYADCLAGTY SGGNKRKLST AIALIGCPPL VLLDEPTTGM DPQARRMLWN VIVSIIREGR
AVVLTSHSME ECEALCTRLA IMVKGAFRCM GTIQHLKSKF GDGYIVTMKI KSPKDDLLPD
LNPVEQFFQG NFPGSVQRER HYNMLQFQVS SSSLARIFQL LLSHKDSLLI EEYSVTQTTL
DQVFVNFAKQ QTESHDLPLH PRAAGASRQA QD*
mutated AA sequence MVVEGVVYFL LTLLVQRHFF LSQWIAEPTK EPIVDEDDDV AEERQRIITG GNKTDILRLH
ELTKIYPGTS SPAVDRLCVG VRPGECFGLL GVNGAGKTTT FKMLTGDTTV TSGDATVAGK
SILTNISEVH QNMGYCPQFD AIDELFTGRE HLYLYARLRG VPAEEIEKVA NWSIKSLGLT
VYADCLAGTY SGGNKRKLST AIALIGCPPL VLLDEPTTGM DPQARRMLWN VIVSIIREGR
AVVLTSHSME ECEALCTRLA IMVKGAFRCM GTIQHLKSKF GDGYIVTMKI KSPKDDLLPD
LNPVEQFFQG NFPGSVQRER HYNMLQFQVS SSSLARIFQL LLSHKDSLLI EEYSVTQTTL
DQVFVNFAKQ QTESHDLPLH PRAAGASRQA QD*
speed 1.41 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
back to results table
Yum, tasty mutations...

mutation t@sting

 documentation

Prediction

disease causing

 Model: simple_aae, prob: 0.999999843789528 (classification due to ClinVar, real probability is shown anyway)      (explain)
Summary
  • amino acid sequence changed
  • known disease mutation at this position (HGMD CM970018)
  • known disease mutation: rs7882 (pathogenic)
  • protein features (might be) affected
 hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr1:94471065G>AN/A show variant in all transcripts   IGV
HGNC symbol ABCA4
Ensembl transcript ID ENST00000370225
Genbank transcript ID NM_000350
UniProt peptide P78363
alteration type single base exchange
alteration region CDS
DNA changes c.6079C>T
cDNA.6166C>T
g.115624C>T
AA changes L2027F Score: 22 explain score(s)
position(s) of altered AA
if AA alteration in CDS		 2027
frameshift no
known variant Reference ID: rs61751408
databasehomozygous (A/A)heterozygousallele carriers
1000G011
ExAC02626

known disease mutation: rs7882 (pathogenic for Retinal dystrophy|Age-related macular degeneration 2|Stargardt disease 1|Retinitis pigmentosa 19|Cone-rod dystrophy 3|Stargardt disease|not provided) dbSNP  NCBI variation viewer
known disease mutation at this position, please check HGMD for details (HGMD ID CM970018)

known disease mutation at this position, please check HGMD for details (HGMD ID CM970018)
known disease mutation at this position, please check HGMD for details (HGMD ID CM970018)
regulatory features H3K27me3, Histone, Histone 3 Lysine 27 Tri-Methylation
H3K4me1, Histone, Histone 3 Lysine 4 Mono-Methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)5.2051
4.6041
(flanking)1.3411
explain score(s) and/or inspect your position(s) in in UCSC Genome Browser
splice sites no abrogation of potential splice sites
distance from splice site 69
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      2027YCPQFDAIDELLTGREHLYLYARL
mutated  not conserved    2027YCPQFDAIDELFTGREHLYLYAR
Ptroglodytes  all identical  ENSPTRG00000023377  2027YCPQFDAIDELLTGREHLYLYAR
Mmulatta  all identical  ENSMMUG00000013858  1018MCPQHNILFHHLTVAEHILFYAQ
Fcatus  no homologue    
Mmusculus  all identical  ENSMUSG00000028125  2026YCPQFDAIDDLLTGREHLYLYAR
Ggallus  all identical  ENSGALG00000005752  2021YCPQFDALDDLLTGRE
Trubripes  no homologue    
Drerio  all identical  ENSDARG00000062661  2092YCPQFDAIDELLTGREHLYLYAR
Dmelanogaster  no homologue    
Celegans  no homologue    
Xtropicalis  all identical  ENSXETG00000008223  2102IDDLLTGREHLQLYGR
protein features
start (aa)end (aa)featuredetails 
18952273TOPO_DOMCytoplasmic.lost
19382170DOMAINABC transporter 2.lost
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 6822 / 6822
position (AA) of stopcodon in wt / mu AA sequence 2274 / 2274
position of stopcodon in wt / mu cDNA 6909 / 6909
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 88 / 88
chromosome 1
strand -1
last intron/exon boundary 6904
theoretical NMD boundary in CDS 6766
length of CDS 6822
coding sequence (CDS) position 6079
cDNA position
(for ins/del: last normal base / first normal base)		 6166
gDNA position
(for ins/del: last normal base / first normal base)		 115624
chromosomal position
(for ins/del: last normal base / first normal base)		 94471065
original gDNA sequence snippet TTGATGCAATTGATGAGCTGCTCACAGGACGAGAACATCTT
altered gDNA sequence snippet TTGATGCAATTGATGAGCTGTTCACAGGACGAGAACATCTT
original cDNA sequence snippet TTGATGCAATTGATGAGCTGCTCACAGGACGAGAACATCTT
altered cDNA sequence snippet TTGATGCAATTGATGAGCTGTTCACAGGACGAGAACATCTT
wildtype AA sequence MGFVRQIQLL LWKNWTLRKR QKIRFVVELV WPLSLFLVLI WLRNANPLYS HHECHFPNKA
MPSAGMLPWL QGIFCNVNNP CFQSPTPGES PGIVSNYNNS ILARVYRDFQ ELLMNAPESQ
HLGRIWTELH ILSQFMDTLR THPERIAGRG IRIRDILKDE ETLTLFLIKN IGLSDSVVYL
LINSQVRPEQ FAHGVPDLAL KDIACSEALL ERFIIFSQRR GAKTVRYALC SLSQGTLQWI
EDTLYANVDF FKLFRVLPTL LDSRSQGINL RSWGGILSDM SPRIQEFIHR PSMQDLLWVT
RPLMQNGGPE TFTKLMGILS DLLCGYPEGG GSRVLSFNWY EDNNYKAFLG IDSTRKDPIY
SYDRRTTSFC NALIQSLESN PLTKIAWRAA KPLLMGKILY TPDSPAARRI LKNANSTFEE
LEHVRKLVKA WEEVGPQIWY FFDNSTQMNM IRDTLGNPTV KDFLNRQLGE EGITAEAILN
FLYKGPRESQ ADDMANFDWR DIFNITDRTL RLVNQYLECL VLDKFESYND ETQLTQRALS
LLEENMFWAG VVFPDMYPWT SSLPPHVKYK IRMDIDVVEK TNKIKDRYWD SGPRADPVED
FRYIWGGFAY LQDMVEQGIT RSQVQAEAPV GIYLQQMPYP CFVDDSFMII LNRCFPIFMV
LAWIYSVSMT VKSIVLEKEL RLKETLKNQG VSNAVIWCTW FLDSFSIMSM SIFLLTIFIM
HGRILHYSDP FILFLFLLAF STATIMLCFL LSTFFSKASL AAACSGVIYF TLYLPHILCF
AWQDRMTAEL KKAVSLLSPV AFGFGTEYLV RFEEQGLGLQ WSNIGNSPTE GDEFSFLLSM
QMMLLDAAVY GLLAWYLDQV FPGDYGTPLP WYFLLQESYW LGGEGCSTRE ERALEKTEPL
TEETEDPEHP EGIHDSFFER EHPGWVPGVC VKNLVKIFEP CGRPAVDRLN ITFYENQITA
FLGHNGAGKT TTLSILTGLL PPTSGTVLVG GRDIETSLDA VRQSLGMCPQ HNILFHHLTV
AEHMLFYAQL KGKSQEEAQL EMEAMLEDTG LHHKRNEEAQ DLSGGMQRKL SVAIAFVGDA
KVVILDEPTS GVDPYSRRSI WDLLLKYRSG RTIIMSTHHM DEADLLGDRI AIIAQGRLYC
SGTPLFLKNC FGTGLYLTLV RKMKNIQSQR KGSEGTCSCS SKGFSTTCPA HVDDLTPEQV
LDGDVNELMD VVLHHVPEAK LVECIGQELI FLLPNKNFKH RAYASLFREL EETLADLGLS
SFGISDTPLE EIFLKVTEDS DSGPLFAGGA QQKRENVNPR HPCLGPREKA GQTPQDSNVC
SPGAPAAHPE GQPPPEPECP GPQLNTGTQL VLQHVQALLV KRFQHTIRSH KDFLAQIVLP
ATFVFLALML SIVIPPFGEY PALTLHPWIY GQQYTFFSMD EPGSEQFTVL ADVLLNKPGF
GNRCLKEGWL PEYPCGNSTP WKTPSVSPNI TQLFQKQKWT QVNPSPSCRC STREKLTMLP
ECPEGAGGLP PPQRTQRSTE ILQDLTDRNI SDFLVKTYPA LIRSSLKSKF WVNEQRYGGI
SIGGKLPVVP ITGEALVGFL SDLGRIMNVS GGPITREASK EIPDFLKHLE TEDNIKVWFN
NKGWHALVSF LNVAHNAILR ASLPKDRSPE EYGITVISQP LNLTKEQLSE ITVLTTSVDA
VVAICVIFSM SFVPASFVLY LIQERVNKSK HLQFISGVSP TTYWVTNFLW DIMNYSVSAG
LVVGIFIGFQ KKAYTSPENL PALVALLLLY GWAVIPMMYP ASFLFDVPST AYVALSCANL
FIGINSSAIT FILELFENNR TLLRFNAVLR KLLIVFPHFC LGRGLIDLAL SQAVTDVYAR
FGEEHSANPF HWDLIGKNLF AMVVEGVVYF LLTLLVQRHF FLSQWIAEPT KEPIVDEDDD
VAEERQRIIT GGNKTDILRL HELTKIYPGT SSPAVDRLCV GVRPGECFGL LGVNGAGKTT
TFKMLTGDTT VTSGDATVAG KSILTNISEV HQNMGYCPQF DAIDELLTGR EHLYLYARLR
GVPAEEIEKV ANWSIKSLGL TVYADCLAGT YSGGNKRKLS TAIALIGCPP LVLLDEPTTG
MDPQARRMLW NVIVSIIREG RAVVLTSHSM EECEALCTRL AIMVKGAFRC MGTIQHLKSK
FGDGYIVTMK IKSPKDDLLP DLNPVEQFFQ GNFPGSVQRE RHYNMLQFQV SSSSLARIFQ
LLLSHKDSLL IEEYSVTQTT LDQVFVNFAK QQTESHDLPL HPRAAGASRQ AQD*
mutated AA sequence MGFVRQIQLL LWKNWTLRKR QKIRFVVELV WPLSLFLVLI WLRNANPLYS HHECHFPNKA
MPSAGMLPWL QGIFCNVNNP CFQSPTPGES PGIVSNYNNS ILARVYRDFQ ELLMNAPESQ
HLGRIWTELH ILSQFMDTLR THPERIAGRG IRIRDILKDE ETLTLFLIKN IGLSDSVVYL
LINSQVRPEQ FAHGVPDLAL KDIACSEALL ERFIIFSQRR GAKTVRYALC SLSQGTLQWI
EDTLYANVDF FKLFRVLPTL LDSRSQGINL RSWGGILSDM SPRIQEFIHR PSMQDLLWVT
RPLMQNGGPE TFTKLMGILS DLLCGYPEGG GSRVLSFNWY EDNNYKAFLG IDSTRKDPIY
SYDRRTTSFC NALIQSLESN PLTKIAWRAA KPLLMGKILY TPDSPAARRI LKNANSTFEE
LEHVRKLVKA WEEVGPQIWY FFDNSTQMNM IRDTLGNPTV KDFLNRQLGE EGITAEAILN
FLYKGPRESQ ADDMANFDWR DIFNITDRTL RLVNQYLECL VLDKFESYND ETQLTQRALS
LLEENMFWAG VVFPDMYPWT SSLPPHVKYK IRMDIDVVEK TNKIKDRYWD SGPRADPVED
FRYIWGGFAY LQDMVEQGIT RSQVQAEAPV GIYLQQMPYP CFVDDSFMII LNRCFPIFMV
LAWIYSVSMT VKSIVLEKEL RLKETLKNQG VSNAVIWCTW FLDSFSIMSM SIFLLTIFIM
HGRILHYSDP FILFLFLLAF STATIMLCFL LSTFFSKASL AAACSGVIYF TLYLPHILCF
AWQDRMTAEL KKAVSLLSPV AFGFGTEYLV RFEEQGLGLQ WSNIGNSPTE GDEFSFLLSM
QMMLLDAAVY GLLAWYLDQV FPGDYGTPLP WYFLLQESYW LGGEGCSTRE ERALEKTEPL
TEETEDPEHP EGIHDSFFER EHPGWVPGVC VKNLVKIFEP CGRPAVDRLN ITFYENQITA
FLGHNGAGKT TTLSILTGLL PPTSGTVLVG GRDIETSLDA VRQSLGMCPQ HNILFHHLTV
AEHMLFYAQL KGKSQEEAQL EMEAMLEDTG LHHKRNEEAQ DLSGGMQRKL SVAIAFVGDA
KVVILDEPTS GVDPYSRRSI WDLLLKYRSG RTIIMSTHHM DEADLLGDRI AIIAQGRLYC
SGTPLFLKNC FGTGLYLTLV RKMKNIQSQR KGSEGTCSCS SKGFSTTCPA HVDDLTPEQV
LDGDVNELMD VVLHHVPEAK LVECIGQELI FLLPNKNFKH RAYASLFREL EETLADLGLS
SFGISDTPLE EIFLKVTEDS DSGPLFAGGA QQKRENVNPR HPCLGPREKA GQTPQDSNVC
SPGAPAAHPE GQPPPEPECP GPQLNTGTQL VLQHVQALLV KRFQHTIRSH KDFLAQIVLP
ATFVFLALML SIVIPPFGEY PALTLHPWIY GQQYTFFSMD EPGSEQFTVL ADVLLNKPGF
GNRCLKEGWL PEYPCGNSTP WKTPSVSPNI TQLFQKQKWT QVNPSPSCRC STREKLTMLP
ECPEGAGGLP PPQRTQRSTE ILQDLTDRNI SDFLVKTYPA LIRSSLKSKF WVNEQRYGGI
SIGGKLPVVP ITGEALVGFL SDLGRIMNVS GGPITREASK EIPDFLKHLE TEDNIKVWFN
NKGWHALVSF LNVAHNAILR ASLPKDRSPE EYGITVISQP LNLTKEQLSE ITVLTTSVDA
VVAICVIFSM SFVPASFVLY LIQERVNKSK HLQFISGVSP TTYWVTNFLW DIMNYSVSAG
LVVGIFIGFQ KKAYTSPENL PALVALLLLY GWAVIPMMYP ASFLFDVPST AYVALSCANL
FIGINSSAIT FILELFENNR TLLRFNAVLR KLLIVFPHFC LGRGLIDLAL SQAVTDVYAR
FGEEHSANPF HWDLIGKNLF AMVVEGVVYF LLTLLVQRHF FLSQWIAEPT KEPIVDEDDD
VAEERQRIIT GGNKTDILRL HELTKIYPGT SSPAVDRLCV GVRPGECFGL LGVNGAGKTT
TFKMLTGDTT VTSGDATVAG KSILTNISEV HQNMGYCPQF DAIDELFTGR EHLYLYARLR
GVPAEEIEKV ANWSIKSLGL TVYADCLAGT YSGGNKRKLS TAIALIGCPP LVLLDEPTTG
MDPQARRMLW NVIVSIIREG RAVVLTSHSM EECEALCTRL AIMVKGAFRC MGTIQHLKSK
FGDGYIVTMK IKSPKDDLLP DLNPVEQFFQ GNFPGSVQRE RHYNMLQFQV SSSSLARIFQ
LLLSHKDSLL IEEYSVTQTT LDQVFVNFAK QQTESHDLPL HPRAAGASRQ AQD*
speed 1.38 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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Problems