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 5 transcript(s)...
Querying Taster for transcript #1: ENST00000543189
Querying Taster for transcript #2: ENST00000536444
Querying Taster for transcript #3: ENST00000544627
Querying Taster for transcript #4: ENST00000540793
Querying Taster for transcript #5: ENST00000261168
MT speed 0 s - this script 6.077064 s

Results

genesymbolpredictionprobabilitymodelprediction
problem		splicingClinVaramino acid changesvariant typedbSNP IDprotein lengthfile
ATF7IPpolymorphism_automatic3.86024545662167e-13simple_aaeN356Isingle base exchangers2231909show file
ATF7IPpolymorphism_automatic1.54698476251269e-12simple_aaeN348Isingle base exchangers2231909show file
ATF7IPpolymorphism_automatic1.54698476251269e-12simple_aaeN348Isingle base exchangers2231909show file
ATF7IPpolymorphism_automatic1.54698476251269e-12simple_aaeN348Isingle base exchangers2231909show file
ATF7IPpolymorphism_automatic1.54698476251269e-12simple_aaeN348Isingle base exchangers2231909show file

Taster files

Yum, tasty mutations...

mutation t@sting

 documentation

Prediction

polymorphism

 Model: simple_aae, prob: 0.999999999999614 (classification due to TGP/ExAC, real probability is shown anyway)      (explain)
Summary
  • amino acid sequence changed
  • homozygous in TGP or ExAC
  • protein features (might be) affected
 hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr12:14577892A>TN/A show variant in all transcripts   IGV
HGNC symbol ATF7IP
Ensembl transcript ID ENST00000544627
Genbank transcript ID N/A
UniProt peptide Q6VMQ6
alteration type single base exchange
alteration region CDS
DNA changes c.1067A>T
cDNA.1387A>T
g.59283A>T
AA changes N356I Score: 149 explain score(s)
position(s) of altered AA
if AA alteration in CDS		 356
frameshift no
known variant Reference ID: rs2231909
databasehomozygous (T/T)heterozygousallele carriers
1000G3059991304
ExAC93031416123464
regulatory features H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)0.2120.001
0.0380.008
(flanking)-0.0770.039
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 516
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      356EKNKADNNIDANEETLETDDTTIC
mutated  not conserved    356EKNKADNNIDAIEETL
Ptroglodytes  all identical  ENSPTRG00000004719  348EKNKTDNNIDANEETLETDDTTI
Mmulatta  all identical  ENSMMUG00000003664  356EKNKADNNIDANEETL
Fcatus  all conserved  ENSFCAG00000010546  321EKNKADSNVDGDEETLETDDTVI
Mmusculus  not conserved  ENSMUSG00000030213  386EGNKVNSNVVEKEEPLETHSAII
Ggallus  not conserved  ENSGALG00000011814  166ENKSNCDNSFSPEEKGKTNDITI
Trubripes  no alignment  ENSTRUG00000000026  n/a
Drerio  no alignment  ENSDARG00000069619  n/a
Dmelanogaster  no homologue    
Celegans  no homologue    
Xtropicalis  not conserved  ENSXETG00000031812  331EKSE---NVETTAENIETP----
protein features
start (aa)end (aa)featuredetails 
349580COMPBIASGlu-rich.lost
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 3837 / 3837
position (AA) of stopcodon in wt / mu AA sequence 1279 / 1279
position of stopcodon in wt / mu cDNA 4157 / 4157
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 321 / 321
chromosome 12
strand 1
last intron/exon boundary 3738
theoretical NMD boundary in CDS 3367
length of CDS 3837
coding sequence (CDS) position 1067
cDNA position
(for ins/del: last normal base / first normal base)		 1387
gDNA position
(for ins/del: last normal base / first normal base)		 59283
chromosomal position
(for ins/del: last normal base / first normal base)		 14577892
original gDNA sequence snippet TGATAATAATATTGATGCTAATGAAGAAACTCTAGAAACAG
altered gDNA sequence snippet TGATAATAATATTGATGCTATTGAAGAAACTCTAGAAACAG
original cDNA sequence snippet TGATAATAATATTGATGCTAATGAAGAAACTCTAGAAACAG
altered cDNA sequence snippet TGATAATAATATTGATGCTATTGAAGAAACTCTAGAAACAG
wildtype AA sequence MHQDQRFRMD SLEEPQKKVF KARKTMRVSD RQQLEAVYKV KEELLKTDVK LLNGNHENGD
LDPTSPLENM DYIKDKEEVN GIEEICFDPE GSKAEWKETP CILSVNVKNK QDDDLNCEPL
SPHNITPEPV SKLPAEPVSG DPAPGDLDAG DPASGVLASG DSTSGDPTSS EPSSSDAASG
DATSGDAPSG DVSPGDATSG DATADDLSSG DPTSSDPIPG EPVPVEPISG DCAADDIASS
EITSVDLASG APASTDPASD DLASGDLSSS ELASDDLATG ELASDELTSE STFDRTFEPK
SVPVCEPVPE IDNIEPSSNK DDDFLEKNGA DEKLEQIQSK DSLDEKNKAD NNIDANEETL
ETDDTTICSD RPPENEKKVE EDIITELALG EDAISSSMEI DQGEKNEDET SADLVETINE
NVIEDNKSEN ILENTDSMET DEIIPILEKL APSEDELTCF SKTSLLPIDE TNPDLEEKME
SSFGSPSKQE SSESLPKEAF LVLSDEEDIS GEKDESEVIS QNETCSPAEV ESNEKDNKPE
EEEQVIHEDD ERPSEKNEFS RRKRSKSEDM DNVQSKRRRY MEEEYEAEFQ VKITAKGDIN
QKLQKVIQWL LEEKLCALQC AVFDKTLAEL KTRVEKIECN KRHKTVLTEL QAKIARLTKR
FEAAKEDLKK RHEHPPNPPV SPGKTVNDVN SNNNMSYRNA GTVRQMLESK RNVSESAPPS
FQTPVNTVSS TNLVTPPAVV SSQPKLQTPV TSGSLTATSV LPAPNTATVV ATTQVPSGNP
QPTISLQPLP VILHVPVAVS SQPQLLQSHP GTLVTNQPSG NVEFISVQSP PTVSGLTKNP
VSLPSLPNPT KPNNVPSVPS PSIQRNPTAS AAPLGTTLAV QAVPTAHSIV QATRTSLPTV
GPSGLYSPST NRGPIQMKIP ISAFSTSSAA EQNSNTTPRI ENQTNKTIDA SVSKKAADST
SQCGKATGSD SSGVIDLTMD DEESGASQDP KKLNHTPVST MSSSQPVSRP LQPIQPAPPL
QPSGVPTSGP SQTTIHLLPT APTTVNVTHR PVTQVTTRLP VPRAPANHQV VYTTLPAPPA
QAPLRGTVMQ APAVRQVNPQ NSVTVRVPQT TTYVVNNGLT LGSTGPQLTV HHRPPQVHTE
PPRPVHPAPL PEAPQPQRLP PEAASTSLPQ KPHLKLARVQ SQNGIVLSWS VLEVDRSCAT
VDSYHLYAYH EEPSATVPSQ WKKIGEVKAL PLPMACTLTQ FVSGSKYYFA VRAKDIYGRF
GPFCDPQSTD VISSTQSS*
mutated AA sequence MHQDQRFRMD SLEEPQKKVF KARKTMRVSD RQQLEAVYKV KEELLKTDVK LLNGNHENGD
LDPTSPLENM DYIKDKEEVN GIEEICFDPE GSKAEWKETP CILSVNVKNK QDDDLNCEPL
SPHNITPEPV SKLPAEPVSG DPAPGDLDAG DPASGVLASG DSTSGDPTSS EPSSSDAASG
DATSGDAPSG DVSPGDATSG DATADDLSSG DPTSSDPIPG EPVPVEPISG DCAADDIASS
EITSVDLASG APASTDPASD DLASGDLSSS ELASDDLATG ELASDELTSE STFDRTFEPK
SVPVCEPVPE IDNIEPSSNK DDDFLEKNGA DEKLEQIQSK DSLDEKNKAD NNIDAIEETL
ETDDTTICSD RPPENEKKVE EDIITELALG EDAISSSMEI DQGEKNEDET SADLVETINE
NVIEDNKSEN ILENTDSMET DEIIPILEKL APSEDELTCF SKTSLLPIDE TNPDLEEKME
SSFGSPSKQE SSESLPKEAF LVLSDEEDIS GEKDESEVIS QNETCSPAEV ESNEKDNKPE
EEEQVIHEDD ERPSEKNEFS RRKRSKSEDM DNVQSKRRRY MEEEYEAEFQ VKITAKGDIN
QKLQKVIQWL LEEKLCALQC AVFDKTLAEL KTRVEKIECN KRHKTVLTEL QAKIARLTKR
FEAAKEDLKK RHEHPPNPPV SPGKTVNDVN SNNNMSYRNA GTVRQMLESK RNVSESAPPS
FQTPVNTVSS TNLVTPPAVV SSQPKLQTPV TSGSLTATSV LPAPNTATVV ATTQVPSGNP
QPTISLQPLP VILHVPVAVS SQPQLLQSHP GTLVTNQPSG NVEFISVQSP PTVSGLTKNP
VSLPSLPNPT KPNNVPSVPS PSIQRNPTAS AAPLGTTLAV QAVPTAHSIV QATRTSLPTV
GPSGLYSPST NRGPIQMKIP ISAFSTSSAA EQNSNTTPRI ENQTNKTIDA SVSKKAADST
SQCGKATGSD SSGVIDLTMD DEESGASQDP KKLNHTPVST MSSSQPVSRP LQPIQPAPPL
QPSGVPTSGP SQTTIHLLPT APTTVNVTHR PVTQVTTRLP VPRAPANHQV VYTTLPAPPA
QAPLRGTVMQ APAVRQVNPQ NSVTVRVPQT TTYVVNNGLT LGSTGPQLTV HHRPPQVHTE
PPRPVHPAPL PEAPQPQRLP PEAASTSLPQ KPHLKLARVQ SQNGIVLSWS VLEVDRSCAT
VDSYHLYAYH EEPSATVPSQ WKKIGEVKAL PLPMACTLTQ FVSGSKYYFA VRAKDIYGRF
GPFCDPQSTD VISSTQSS*
speed 1.39 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

polymorphism

 Model: simple_aae, prob: 0.999999999998453 (classification due to TGP/ExAC, real probability is shown anyway)      (explain)
Summary
  • amino acid sequence changed
  • homozygous in TGP or ExAC
 hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr12:14577892A>TN/A show variant in all transcripts   IGV
HGNC symbol ATF7IP
Ensembl transcript ID ENST00000543189
Genbank transcript ID N/A
UniProt peptide Q6VMQ6
alteration type single base exchange
alteration region CDS
DNA changes c.1043A>T
cDNA.1185A>T
g.59283A>T
AA changes N348I Score: 149 explain score(s)
position(s) of altered AA
if AA alteration in CDS		 348
frameshift no
known variant Reference ID: rs2231909
databasehomozygous (T/T)heterozygousallele carriers
1000G3059991304
ExAC93031416123464
regulatory features H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)0.2120.001
0.0380.008
(flanking)-0.0770.039
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 516
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      348EKNKADNNIDANEETLETDDTTIC
mutated  not conserved    348EKNKADNNIDAIEETLETDDTTI
Ptroglodytes  all identical  ENSPTRG00000004719  348EKNKTDNNIDANEETLETDDTTI
Mmulatta  all identical  ENSMMUG00000003664  356EKNKADNNIDANEETLETDDTTI
Fcatus  all conserved  ENSFCAG00000010546  321EKNKADSNVDGDEETLETDDTVI
Mmusculus  not conserved  ENSMUSG00000030213  386EGNKVNSNVVEKEEPLETHSAII
Ggallus  not conserved  ENSGALG00000011814  166ENKSNCDNSFSPEEKGKTNDITI
Trubripes  no alignment  ENSTRUG00000000026  n/a
Drerio  no alignment  ENSDARG00000069619  n/a
Dmelanogaster  no homologue    
Celegans  no homologue    
Xtropicalis  not conserved  ENSXETG00000031812  331EKSE---NVETTAENIETP----
protein features no protein features affected
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 3318 / 3318
position (AA) of stopcodon in wt / mu AA sequence 1106 / 1106
position of stopcodon in wt / mu cDNA 3460 / 3460
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 143 / 143
chromosome 12
strand 1
last intron/exon boundary 3237
theoretical NMD boundary in CDS 3044
length of CDS 3318
coding sequence (CDS) position 1043
cDNA position
(for ins/del: last normal base / first normal base)		 1185
gDNA position
(for ins/del: last normal base / first normal base)		 59283
chromosomal position
(for ins/del: last normal base / first normal base)		 14577892
original gDNA sequence snippet TGATAATAATATTGATGCTAATGAAGAAACTCTAGAAACAG
altered gDNA sequence snippet TGATAATAATATTGATGCTATTGAAGAAACTCTAGAAACAG
original cDNA sequence snippet TGATAATAATATTGATGCTAATGAAGAAACTCTAGAAACAG
altered cDNA sequence snippet TGATAATAATATTGATGCTATTGAAGAAACTCTAGAAACAG
wildtype AA sequence MDSLEEPQKK VFKARKTMRV SDRQQLEAVY KVKEELLKTD VKLLNGNHEN GDLDPTSPLE
NMDYIKDKEE VNGIEEICFD PEGSKAEWKE TPCILSVNVK NKQDDDLNCE PLSPHNITPE
PVSKLPAEPV SGDPAPGDLD AGDPASGVLA SGDSTSGDPT SSEPSSSDAA SGDATSGDAP
SGDVSPGDAT SGDATADDLS SGDPTSSDPI PGEPVPVEPI SGDCAADDIA SSEITSVDLA
SGAPASTDPA SDDLASGDLS SSELASDDLA TGELASDELT SESTFDRTFE PKSVPVCEPV
PEIDNIEPSS NKDDDFLEKN GADEKLEQIQ SKDSLDEKNK ADNNIDANEE TLETDDTTIC
SDRPPENEKK VEEDIITELA LGEDAISSSM EIDQGEKNED ETSADLVETI NENVIEDNKS
ENILENTDSM ETDEIIPILE KLAPSEDELT CFSKTSLLPI DETNPDLEEK MESSFGSPSK
QESSESLPKE AFLVLSDEED ISGEKDESEV ISQNETCSPE VESNEKDNKP EEEEQVIHED
DERPSEKNEF SRRKRSKSED MDNVQSKRRR YMEEEYEAEF QVKITAKGDI NQKLQKVIQW
LLEEKLCALQ CAVFDKTLAE LKTRVEKIEC NKRHKTVLTE LQAKIARLTK RFEAAKEDLK
KRHEHPPNPP VSPGKTVNDV NSNNNMSYRN AGTVRQMLES KRNVSESAPP SFQTPVNTVS
STNLVTPPAV VSSQPKLQTP VTSGSLTATS VLPAPNTATV VATTQVPSGN PQPTISLQPL
PVILHVPVAV SSQPQLLQSH PGTLVTNQPS GNVEFISVQS PPTVSGLTKN PVSLPSLPNP
TKPNNVPSVP SPSIQRNPTA SAAPLGTTLA VQAVPTAHSI VQATRTSLPT VGPSGLYSPS
TNRGPIQMKI PISAFSTSSA AEQNSNTTPR IENQTNKTID ASVSKKAADS TSQCGKATGS
DSSGVIDLTM DDEESGASQD PKKLNHTPVS TMSSSQPVSR PLQPIQPAPP LQPSGVPTSG
PSQTTIHLLP TAPTTVNVTH RPVTQVTTRL PVPRAPANHQ VVYTTLPAPP AQAPLRGTVM
QAPAVRQVNP QNSKRFFLYM APRYM*
mutated AA sequence MDSLEEPQKK VFKARKTMRV SDRQQLEAVY KVKEELLKTD VKLLNGNHEN GDLDPTSPLE
NMDYIKDKEE VNGIEEICFD PEGSKAEWKE TPCILSVNVK NKQDDDLNCE PLSPHNITPE
PVSKLPAEPV SGDPAPGDLD AGDPASGVLA SGDSTSGDPT SSEPSSSDAA SGDATSGDAP
SGDVSPGDAT SGDATADDLS SGDPTSSDPI PGEPVPVEPI SGDCAADDIA SSEITSVDLA
SGAPASTDPA SDDLASGDLS SSELASDDLA TGELASDELT SESTFDRTFE PKSVPVCEPV
PEIDNIEPSS NKDDDFLEKN GADEKLEQIQ SKDSLDEKNK ADNNIDAIEE TLETDDTTIC
SDRPPENEKK VEEDIITELA LGEDAISSSM EIDQGEKNED ETSADLVETI NENVIEDNKS
ENILENTDSM ETDEIIPILE KLAPSEDELT CFSKTSLLPI DETNPDLEEK MESSFGSPSK
QESSESLPKE AFLVLSDEED ISGEKDESEV ISQNETCSPE VESNEKDNKP EEEEQVIHED
DERPSEKNEF SRRKRSKSED MDNVQSKRRR YMEEEYEAEF QVKITAKGDI NQKLQKVIQW
LLEEKLCALQ CAVFDKTLAE LKTRVEKIEC NKRHKTVLTE LQAKIARLTK RFEAAKEDLK
KRHEHPPNPP VSPGKTVNDV NSNNNMSYRN AGTVRQMLES KRNVSESAPP SFQTPVNTVS
STNLVTPPAV VSSQPKLQTP VTSGSLTATS VLPAPNTATV VATTQVPSGN PQPTISLQPL
PVILHVPVAV SSQPQLLQSH PGTLVTNQPS GNVEFISVQS PPTVSGLTKN PVSLPSLPNP
TKPNNVPSVP SPSIQRNPTA SAAPLGTTLA VQAVPTAHSI VQATRTSLPT VGPSGLYSPS
TNRGPIQMKI PISAFSTSSA AEQNSNTTPR IENQTNKTID ASVSKKAADS TSQCGKATGS
DSSGVIDLTM DDEESGASQD PKKLNHTPVS TMSSSQPVSR PLQPIQPAPP LQPSGVPTSG
PSQTTIHLLP TAPTTVNVTH RPVTQVTTRL PVPRAPANHQ VVYTTLPAPP AQAPLRGTVM
QAPAVRQVNP QNSKRFFLYM APRYM*
speed 1.34 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

polymorphism

 Model: simple_aae, prob: 0.999999999998453 (classification due to TGP/ExAC, real probability is shown anyway)      (explain)
Summary
  • amino acid sequence changed
  • homozygous in TGP or ExAC
 hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr12:14577892A>TN/A show variant in all transcripts   IGV
HGNC symbol ATF7IP
Ensembl transcript ID ENST00000536444
Genbank transcript ID N/A
UniProt peptide Q6VMQ6
alteration type single base exchange
alteration region CDS
DNA changes c.1043A>T
cDNA.1149A>T
g.59283A>T
AA changes N348I Score: 149 explain score(s)
position(s) of altered AA
if AA alteration in CDS		 348
frameshift no
known variant Reference ID: rs2231909
databasehomozygous (T/T)heterozygousallele carriers
1000G3059991304
ExAC93031416123464
regulatory features H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)0.2120.001
0.0380.008
(flanking)-0.0770.039
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 516
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      348EKNKADNNIDANEETLETDDTTIC
mutated  not conserved    348EKNKADNNIDAIEETLETDDTTI
Ptroglodytes  all identical  ENSPTRG00000004719  348EKNKTDNNIDANEETLETDDTTI
Mmulatta  all identical  ENSMMUG00000003664  356EKNKADNNIDANEETLETDDTTI
Fcatus  all conserved  ENSFCAG00000010546  321EKNKADSNVDGDEETLETDDTVI
Mmusculus  not conserved  ENSMUSG00000030213  386EGNKVNSNVVEKEEPLETHSAII
Ggallus  not conserved  ENSGALG00000011814  166ENKSNCDNSFSPEEKGKTNDITI
Trubripes  no alignment  ENSTRUG00000000026  n/a
Drerio  no alignment  ENSDARG00000069619  n/a
Dmelanogaster  no homologue    
Celegans  no homologue    
Xtropicalis  not conserved  ENSXETG00000031812  331EKSE---NVETTAENIETP----
protein features no protein features affected
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 3810 / 3810
position (AA) of stopcodon in wt / mu AA sequence 1270 / 1270
position of stopcodon in wt / mu cDNA 3916 / 3916
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 107 / 107
chromosome 12
strand 1
last intron/exon boundary 3497
theoretical NMD boundary in CDS 3340
length of CDS 3810
coding sequence (CDS) position 1043
cDNA position
(for ins/del: last normal base / first normal base)		 1149
gDNA position
(for ins/del: last normal base / first normal base)		 59283
chromosomal position
(for ins/del: last normal base / first normal base)		 14577892
original gDNA sequence snippet TGATAATAATATTGATGCTAATGAAGAAACTCTAGAAACAG
altered gDNA sequence snippet TGATAATAATATTGATGCTATTGAAGAAACTCTAGAAACAG
original cDNA sequence snippet TGATAATAATATTGATGCTAATGAAGAAACTCTAGAAACAG
altered cDNA sequence snippet TGATAATAATATTGATGCTATTGAAGAAACTCTAGAAACAG
wildtype AA sequence MDSLEEPQKK VFKARKTMRV SDRQQLEAVY KVKEELLKTD VKLLNGNHEN GDLDPTSPLE
NMDYIKDKEE VNGIEEICFD PEGSKAEWKE TPCILSVNVK NKQDDDLNCE PLSPHNITPE
PVSKLPAEPV SGDPAPGDLD AGDPASGVLA SGDSTSGDPT SSEPSSSDAA SGDATSGDAP
SGDVSPGDAT SGDATADDLS SGDPTSSDPI PGEPVPVEPI SGDCAADDIA SSEITSVDLA
SGAPASTDPA SDDLASGDLS SSELASDDLA TGELASDELT SESTFDRTFE PKSVPVCEPV
PEIDNIEPSS NKDDDFLEKN GADEKLEQIQ SKDSLDEKNK ADNNIDANEE TLETDDTTIC
SDRPPENEKK VEEDIITELA LGEDAISSSM EIDQGEKNED ETSADLVETI NENVIEDNKS
ENILENTDSM ETDEIIPILE KLAPSEDELT CFSKTSLLPI DETNPDLEEK MESSFGSPSK
QESSESLPKE AFLVLSDEED ISGEKDESEV ISQNETCSPE VESNEKDNKP EEEEQVIHED
DERPSEKNEF SRRKRSKSED MDNVQSKRRR YMEEEYEAEF QVKITAKGDI NQKLQKVIQW
LLEEKLCALQ CAVFDKTLAE LKTRVEKIEC NKRHKTVLTE LQAKIARLTK RFEAAKEDLK
KRHEHPPNPP VSPGKTVNDV NSNNNMSYRN AGTVRQMLES KRNVSESAPP SFQTPVNTVS
STNLVTPPAV VSSQPKLQTP VTSGSLTATS VLPAPNTATV VATTQVPSGN PQPTISLQPL
PVILHVPVAV SSQPQLLQSH PGTLVTNQPS GNVEFISVQS PPTVSGLTKN PVSLPSLPNP
TKPNNVPSVP SPSIQRNPTA SAAPLGTTLA VQAVPTAHSI VQATRTSLPT VGPSGLYSPS
TNRGPIQMKI PISAFSTSSA AEQNSNTTPR IENQTNKTID ASVSKKAADS TSQCGKATGS
DSSGVIDLTM DDEESGASQD PKKLNHTPVS TMSSSQPVSR PLQPIQPAPP LQPSGVPTSG
PSQTTIHLLP TAPTTVNVTH RPVTQVTTRL PVPRAPANHQ VVYTTLPAPP AQAPLRGTVM
QAPAVRQVNP QNSVTVRVPQ TTTYVVNNGL TLGSTGPQLT VHHRPPQVHT EPPRPVHPAP
LPEAPQPQRL PPEAASTSLP QKPHLKLARV QSQNGIVLSW SVLEVDRSCA TVDSYHLYAY
HEEPSATVPS QWKKIGEVKA LPLPMACTLT QFVSGSKYYF AVRAKDIYGR FGPFCDPQST
DVISSTQSS*
mutated AA sequence MDSLEEPQKK VFKARKTMRV SDRQQLEAVY KVKEELLKTD VKLLNGNHEN GDLDPTSPLE
NMDYIKDKEE VNGIEEICFD PEGSKAEWKE TPCILSVNVK NKQDDDLNCE PLSPHNITPE
PVSKLPAEPV SGDPAPGDLD AGDPASGVLA SGDSTSGDPT SSEPSSSDAA SGDATSGDAP
SGDVSPGDAT SGDATADDLS SGDPTSSDPI PGEPVPVEPI SGDCAADDIA SSEITSVDLA
SGAPASTDPA SDDLASGDLS SSELASDDLA TGELASDELT SESTFDRTFE PKSVPVCEPV
PEIDNIEPSS NKDDDFLEKN GADEKLEQIQ SKDSLDEKNK ADNNIDAIEE TLETDDTTIC
SDRPPENEKK VEEDIITELA LGEDAISSSM EIDQGEKNED ETSADLVETI NENVIEDNKS
ENILENTDSM ETDEIIPILE KLAPSEDELT CFSKTSLLPI DETNPDLEEK MESSFGSPSK
QESSESLPKE AFLVLSDEED ISGEKDESEV ISQNETCSPE VESNEKDNKP EEEEQVIHED
DERPSEKNEF SRRKRSKSED MDNVQSKRRR YMEEEYEAEF QVKITAKGDI NQKLQKVIQW
LLEEKLCALQ CAVFDKTLAE LKTRVEKIEC NKRHKTVLTE LQAKIARLTK RFEAAKEDLK
KRHEHPPNPP VSPGKTVNDV NSNNNMSYRN AGTVRQMLES KRNVSESAPP SFQTPVNTVS
STNLVTPPAV VSSQPKLQTP VTSGSLTATS VLPAPNTATV VATTQVPSGN PQPTISLQPL
PVILHVPVAV SSQPQLLQSH PGTLVTNQPS GNVEFISVQS PPTVSGLTKN PVSLPSLPNP
TKPNNVPSVP SPSIQRNPTA SAAPLGTTLA VQAVPTAHSI VQATRTSLPT VGPSGLYSPS
TNRGPIQMKI PISAFSTSSA AEQNSNTTPR IENQTNKTID ASVSKKAADS TSQCGKATGS
DSSGVIDLTM DDEESGASQD PKKLNHTPVS TMSSSQPVSR PLQPIQPAPP LQPSGVPTSG
PSQTTIHLLP TAPTTVNVTH RPVTQVTTRL PVPRAPANHQ VVYTTLPAPP AQAPLRGTVM
QAPAVRQVNP QNSVTVRVPQ TTTYVVNNGL TLGSTGPQLT VHHRPPQVHT EPPRPVHPAP
LPEAPQPQRL PPEAASTSLP QKPHLKLARV QSQNGIVLSW SVLEVDRSCA TVDSYHLYAY
HEEPSATVPS QWKKIGEVKA LPLPMACTLT QFVSGSKYYF AVRAKDIYGR FGPFCDPQST
DVISSTQSS*
speed 0.83 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

polymorphism

 Model: simple_aae, prob: 0.999999999998453 (classification due to TGP/ExAC, real probability is shown anyway)      (explain)
Summary
  • amino acid sequence changed
  • homozygous in TGP or ExAC
 hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr12:14577892A>TN/A show variant in all transcripts   IGV
HGNC symbol ATF7IP
Ensembl transcript ID ENST00000540793
Genbank transcript ID N/A
UniProt peptide Q6VMQ6
alteration type single base exchange
alteration region CDS
DNA changes c.1043A>T
cDNA.1198A>T
g.59283A>T
AA changes N348I Score: 149 explain score(s)
position(s) of altered AA
if AA alteration in CDS		 348
frameshift no
known variant Reference ID: rs2231909
databasehomozygous (T/T)heterozygousallele carriers
1000G3059991304
ExAC93031416123464
regulatory features H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)0.2120.001
0.0380.008
(flanking)-0.0770.039
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 516
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      348EKNKADNNIDANEETLETDDTTIC
mutated  not conserved    348EKNKADNNIDAIEETLETDDTTI
Ptroglodytes  all identical  ENSPTRG00000004719  348EKNKTDNNIDANEETLETDDTTI
Mmulatta  all identical  ENSMMUG00000003664  356EKNKADNNIDANEETLETDDTTI
Fcatus  all conserved  ENSFCAG00000010546  321EKNKADSNVDGDEETLETDDTVI
Mmusculus  not conserved  ENSMUSG00000030213  386EGNKVNSNVVEKEEPLETHSAII
Ggallus  not conserved  ENSGALG00000011814  166ENKSNCDNSFSPEEKGKTNDITI
Trubripes  no alignment  ENSTRUG00000000026  n/a
Drerio  no alignment  ENSDARG00000069619  n/a
Dmelanogaster  no homologue    
Celegans  no homologue    
Xtropicalis  not conserved  ENSXETG00000031812  331EKSE---NVETTAENIETP----
protein features no protein features affected
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 3813 / 3813
position (AA) of stopcodon in wt / mu AA sequence 1271 / 1271
position of stopcodon in wt / mu cDNA 3968 / 3968
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 156 / 156
chromosome 12
strand 1
last intron/exon boundary 3549
theoretical NMD boundary in CDS 3343
length of CDS 3813
coding sequence (CDS) position 1043
cDNA position
(for ins/del: last normal base / first normal base)		 1198
gDNA position
(for ins/del: last normal base / first normal base)		 59283
chromosomal position
(for ins/del: last normal base / first normal base)		 14577892
original gDNA sequence snippet TGATAATAATATTGATGCTAATGAAGAAACTCTAGAAACAG
altered gDNA sequence snippet TGATAATAATATTGATGCTATTGAAGAAACTCTAGAAACAG
original cDNA sequence snippet TGATAATAATATTGATGCTAATGAAGAAACTCTAGAAACAG
altered cDNA sequence snippet TGATAATAATATTGATGCTATTGAAGAAACTCTAGAAACAG
wildtype AA sequence MDSLEEPQKK VFKARKTMRV SDRQQLEAVY KVKEELLKTD VKLLNGNHEN GDLDPTSPLE
NMDYIKDKEE VNGIEEICFD PEGSKAEWKE TPCILSVNVK NKQDDDLNCE PLSPHNITPE
PVSKLPAEPV SGDPAPGDLD AGDPASGVLA SGDSTSGDPT SSEPSSSDAA SGDATSGDAP
SGDVSPGDAT SGDATADDLS SGDPTSSDPI PGEPVPVEPI SGDCAADDIA SSEITSVDLA
SGAPASTDPA SDDLASGDLS SSELASDDLA TGELASDELT SESTFDRTFE PKSVPVCEPV
PEIDNIEPSS NKDDDFLEKN GADEKLEQIQ SKDSLDEKNK ADNNIDANEE TLETDDTTIC
SDRPPENEKK VEEDIITELA LGEDAISSSM EIDQGEKNED ETSADLVETI NENVIEDNKS
ENILENTDSM ETDEIIPILE KLAPSEDELT CFSKTSLLPI DETNPDLEEK MESSFGSPSK
QESSESLPKE AFLVLSDEED ISGEKDESEV ISQNETCSPA EVESNEKDNK PEEEEQVIHE
DDERPSEKNE FSRRKRSKSE DMDNVQSKRR RYMEEEYEAE FQVKITAKGD INQKLQKVIQ
WLLEEKLCAL QCAVFDKTLA ELKTRVEKIE CNKRHKTVLT ELQAKIARLT KRFEAAKEDL
KKRHEHPPNP PVSPGKTVND VNSNNNMSYR NAGTVRQMLE SKRNVSESAP PSFQTPVNTV
SSTNLVTPPA VVSSQPKLQT PVTSGSLTAT SVLPAPNTAT VVATTQVPSG NPQPTISLQP
LPVILHVPVA VSSQPQLLQS HPGTLVTNQP SGNVEFISVQ SPPTVSGLTK NPVSLPSLPN
PTKPNNVPSV PSPSIQRNPT ASAAPLGTTL AVQAVPTAHS IVQATRTSLP TVGPSGLYSP
STNRGPIQMK IPISAFSTSS AAEQNSNTTP RIENQTNKTI DASVSKKAAD STSQCGKATG
SDSSGVIDLT MDDEESGASQ DPKKLNHTPV STMSSSQPVS RPLQPIQPAP PLQPSGVPTS
GPSQTTIHLL PTAPTTVNVT HRPVTQVTTR LPVPRAPANH QVVYTTLPAP PAQAPLRGTV
MQAPAVRQVN PQNSVTVRVP QTTTYVVNNG LTLGSTGPQL TVHHRPPQVH TEPPRPVHPA
PLPEAPQPQR LPPEAASTSL PQKPHLKLAR VQSQNGIVLS WSVLEVDRSC ATVDSYHLYA
YHEEPSATVP SQWKKIGEVK ALPLPMACTL TQFVSGSKYY FAVRAKDIYG RFGPFCDPQS
TDVISSTQSS *
mutated AA sequence MDSLEEPQKK VFKARKTMRV SDRQQLEAVY KVKEELLKTD VKLLNGNHEN GDLDPTSPLE
NMDYIKDKEE VNGIEEICFD PEGSKAEWKE TPCILSVNVK NKQDDDLNCE PLSPHNITPE
PVSKLPAEPV SGDPAPGDLD AGDPASGVLA SGDSTSGDPT SSEPSSSDAA SGDATSGDAP
SGDVSPGDAT SGDATADDLS SGDPTSSDPI PGEPVPVEPI SGDCAADDIA SSEITSVDLA
SGAPASTDPA SDDLASGDLS SSELASDDLA TGELASDELT SESTFDRTFE PKSVPVCEPV
PEIDNIEPSS NKDDDFLEKN GADEKLEQIQ SKDSLDEKNK ADNNIDAIEE TLETDDTTIC
SDRPPENEKK VEEDIITELA LGEDAISSSM EIDQGEKNED ETSADLVETI NENVIEDNKS
ENILENTDSM ETDEIIPILE KLAPSEDELT CFSKTSLLPI DETNPDLEEK MESSFGSPSK
QESSESLPKE AFLVLSDEED ISGEKDESEV ISQNETCSPA EVESNEKDNK PEEEEQVIHE
DDERPSEKNE FSRRKRSKSE DMDNVQSKRR RYMEEEYEAE FQVKITAKGD INQKLQKVIQ
WLLEEKLCAL QCAVFDKTLA ELKTRVEKIE CNKRHKTVLT ELQAKIARLT KRFEAAKEDL
KKRHEHPPNP PVSPGKTVND VNSNNNMSYR NAGTVRQMLE SKRNVSESAP PSFQTPVNTV
SSTNLVTPPA VVSSQPKLQT PVTSGSLTAT SVLPAPNTAT VVATTQVPSG NPQPTISLQP
LPVILHVPVA VSSQPQLLQS HPGTLVTNQP SGNVEFISVQ SPPTVSGLTK NPVSLPSLPN
PTKPNNVPSV PSPSIQRNPT ASAAPLGTTL AVQAVPTAHS IVQATRTSLP TVGPSGLYSP
STNRGPIQMK IPISAFSTSS AAEQNSNTTP RIENQTNKTI DASVSKKAAD STSQCGKATG
SDSSGVIDLT MDDEESGASQ DPKKLNHTPV STMSSSQPVS RPLQPIQPAP PLQPSGVPTS
GPSQTTIHLL PTAPTTVNVT HRPVTQVTTR LPVPRAPANH QVVYTTLPAP PAQAPLRGTV
MQAPAVRQVN PQNSVTVRVP QTTTYVVNNG LTLGSTGPQL TVHHRPPQVH TEPPRPVHPA
PLPEAPQPQR LPPEAASTSL PQKPHLKLAR VQSQNGIVLS WSVLEVDRSC ATVDSYHLYA
YHEEPSATVP SQWKKIGEVK ALPLPMACTL TQFVSGSKYY FAVRAKDIYG RFGPFCDPQS
TDVISSTQSS *
speed 1.35 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

polymorphism

 Model: simple_aae, prob: 0.999999999998453 (classification due to TGP/ExAC, real probability is shown anyway)      (explain)
Summary
  • amino acid sequence changed
  • homozygous in TGP or ExAC
 hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr12:14577892A>TN/A show variant in all transcripts   IGV
HGNC symbol ATF7IP
Ensembl transcript ID ENST00000261168
Genbank transcript ID NM_018179
UniProt peptide Q6VMQ6
alteration type single base exchange
alteration region CDS
DNA changes c.1043A>T
cDNA.1196A>T
g.59283A>T
AA changes N348I Score: 149 explain score(s)
position(s) of altered AA
if AA alteration in CDS		 348
frameshift no
known variant Reference ID: rs2231909
databasehomozygous (T/T)heterozygousallele carriers
1000G3059991304
ExAC93031416123464
regulatory features H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)0.2120.001
0.0380.008
(flanking)-0.0770.039
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 516
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      348EKNKADNNIDANEETLETDDTTIC
mutated  not conserved    348EKNKADNNIDAIEETLETDDTTI
Ptroglodytes  all identical  ENSPTRG00000004719  348EKNKTDNNIDANEETLETDDTTI
Mmulatta  all identical  ENSMMUG00000003664  356EKNKADNNIDANEETLETDDTTI
Fcatus  all conserved  ENSFCAG00000010546  321EKNKADSNVDGDEETLETDDTVI
Mmusculus  not conserved  ENSMUSG00000030213  386EGNKVNSNVVEKEEPLETHSAII
Ggallus  not conserved  ENSGALG00000011814  166ENKSNCDNSFSPEEKGKTNDITI
Trubripes  no alignment  ENSTRUG00000000026  n/a
Drerio  no alignment  ENSDARG00000069619  n/a
Dmelanogaster  no homologue    
Celegans  no homologue    
Xtropicalis  not conserved  ENSXETG00000031812  331EKSE---NVETTAENIETP----
protein features no protein features affected
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 3813 / 3813
position (AA) of stopcodon in wt / mu AA sequence 1271 / 1271
position of stopcodon in wt / mu cDNA 3966 / 3966
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 154 / 154
chromosome 12
strand 1
last intron/exon boundary 3547
theoretical NMD boundary in CDS 3343
length of CDS 3813
coding sequence (CDS) position 1043
cDNA position
(for ins/del: last normal base / first normal base)		 1196
gDNA position
(for ins/del: last normal base / first normal base)		 59283
chromosomal position
(for ins/del: last normal base / first normal base)		 14577892
original gDNA sequence snippet TGATAATAATATTGATGCTAATGAAGAAACTCTAGAAACAG
altered gDNA sequence snippet TGATAATAATATTGATGCTATTGAAGAAACTCTAGAAACAG
original cDNA sequence snippet TGATAATAATATTGATGCTAATGAAGAAACTCTAGAAACAG
altered cDNA sequence snippet TGATAATAATATTGATGCTATTGAAGAAACTCTAGAAACAG
wildtype AA sequence MDSLEEPQKK VFKARKTMRV SDRQQLEAVY KVKEELLKTD VKLLNGNHEN GDLDPTSPLE
NMDYIKDKEE VNGIEEICFD PEGSKAEWKE TPCILSVNVK NKQDDDLNCE PLSPHNITPE
PVSKLPAEPV SGDPAPGDLD AGDPASGVLA SGDSTSGDPT SSEPSSSDAA SGDATSGDAP
SGDVSPGDAT SGDATADDLS SGDPTSSDPI PGEPVPVEPI SGDCAADDIA SSEITSVDLA
SGAPASTDPA SDDLASGDLS SSELASDDLA TGELASDELT SESTFDRTFE PKSVPVCEPV
PEIDNIEPSS NKDDDFLEKN GADEKLEQIQ SKDSLDEKNK ADNNIDANEE TLETDDTTIC
SDRPPENEKK VEEDIITELA LGEDAISSSM EIDQGEKNED ETSADLVETI NENVIEDNKS
ENILENTDSM ETDEIIPILE KLAPSEDELT CFSKTSLLPI DETNPDLEEK MESSFGSPSK
QESSESLPKE AFLVLSDEED ISGEKDESEV ISQNETCSPA EVESNEKDNK PEEEEQVIHE
DDERPSEKNE FSRRKRSKSE DMDNVQSKRR RYMEEEYEAE FQVKITAKGD INQKLQKVIQ
WLLEEKLCAL QCAVFDKTLA ELKTRVEKIE CNKRHKTVLT ELQAKIARLT KRFEAAKEDL
KKRHEHPPNP PVSPGKTVND VNSNNNMSYR NAGTVRQMLE SKRNVSESAP PSFQTPVNTV
SSTNLVTPPA VVSSQPKLQT PVTSGSLTAT SVLPAPNTAT VVATTQVPSG NPQPTISLQP
LPVILHVPVA VSSQPQLLQS HPGTLVTNQP SGNVEFISVQ SPPTVSGLTK NPVSLPSLPN
PTKPNNVPSV PSPSIQRNPT ASAAPLGTTL AVQAVPTAHS IVQATRTSLP TVGPSGLYSP
STNRGPIQMK IPISAFSTSS AAEQNSNTTP RIENQTNKTI DASVSKKAAD STSQCGKATG
SDSSGVIDLT MDDEESGASQ DPKKLNHTPV STMSSSQPVS RPLQPIQPAP PLQPSGVPTS
GPSQTTIHLL PTAPTTVNVT HRPVTQVTTR LPVPRAPANH QVVYTTLPAP PAQAPLRGTV
MQAPAVRQVN PQNSVTVRVP QTTTYVVNNG LTLGSTGPQL TVHHRPPQVH TEPPRPVHPA
PLPEAPQPQR LPPEAASTSL PQKPHLKLAR VQSQNGIVLS WSVLEVDRSC ATVDSYHLYA
YHEEPSATVP SQWKKIGEVK ALPLPMACTL TQFVSGSKYY FAVRAKDIYG RFGPFCDPQS
TDVISSTQSS *
mutated AA sequence MDSLEEPQKK VFKARKTMRV SDRQQLEAVY KVKEELLKTD VKLLNGNHEN GDLDPTSPLE
NMDYIKDKEE VNGIEEICFD PEGSKAEWKE TPCILSVNVK NKQDDDLNCE PLSPHNITPE
PVSKLPAEPV SGDPAPGDLD AGDPASGVLA SGDSTSGDPT SSEPSSSDAA SGDATSGDAP
SGDVSPGDAT SGDATADDLS SGDPTSSDPI PGEPVPVEPI SGDCAADDIA SSEITSVDLA
SGAPASTDPA SDDLASGDLS SSELASDDLA TGELASDELT SESTFDRTFE PKSVPVCEPV
PEIDNIEPSS NKDDDFLEKN GADEKLEQIQ SKDSLDEKNK ADNNIDAIEE TLETDDTTIC
SDRPPENEKK VEEDIITELA LGEDAISSSM EIDQGEKNED ETSADLVETI NENVIEDNKS
ENILENTDSM ETDEIIPILE KLAPSEDELT CFSKTSLLPI DETNPDLEEK MESSFGSPSK
QESSESLPKE AFLVLSDEED ISGEKDESEV ISQNETCSPA EVESNEKDNK PEEEEQVIHE
DDERPSEKNE FSRRKRSKSE DMDNVQSKRR RYMEEEYEAE FQVKITAKGD INQKLQKVIQ
WLLEEKLCAL QCAVFDKTLA ELKTRVEKIE CNKRHKTVLT ELQAKIARLT KRFEAAKEDL
KKRHEHPPNP PVSPGKTVND VNSNNNMSYR NAGTVRQMLE SKRNVSESAP PSFQTPVNTV
SSTNLVTPPA VVSSQPKLQT PVTSGSLTAT SVLPAPNTAT VVATTQVPSG NPQPTISLQP
LPVILHVPVA VSSQPQLLQS HPGTLVTNQP SGNVEFISVQ SPPTVSGLTK NPVSLPSLPN
PTKPNNVPSV PSPSIQRNPT ASAAPLGTTL AVQAVPTAHS IVQATRTSLP TVGPSGLYSP
STNRGPIQMK IPISAFSTSS AAEQNSNTTP RIENQTNKTI DASVSKKAAD STSQCGKATG
SDSSGVIDLT MDDEESGASQ DPKKLNHTPV STMSSSQPVS RPLQPIQPAP PLQPSGVPTS
GPSQTTIHLL PTAPTTVNVT HRPVTQVTTR LPVPRAPANH QVVYTTLPAP PAQAPLRGTV
MQAPAVRQVN PQNSVTVRVP QTTTYVVNNG LTLGSTGPQL TVHHRPPQVH TEPPRPVHPA
PLPEAPQPQR LPPEAASTSL PQKPHLKLAR VQSQNGIVLS WSVLEVDRSC ATVDSYHLYA
YHEEPSATVP SQWKKIGEVK ALPLPMACTL TQFVSGSKYY FAVRAKDIYG RFGPFCDPQS
TDVISSTQSS *
speed 0.49 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

Problems