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 7 transcript(s)...
Querying Taster for transcript #1: ENST00000359273
Querying Taster for transcript #2: ENST00000392109
Querying Taster for transcript #3: ENST00000392110
Querying Taster for transcript #4: ENST00000392111
Querying Taster for transcript #5: ENST00000412366
Querying Taster for transcript #6: ENST00000439945
Querying Taster for transcript #7: ENST00000431802
MT speed 0 s - this script 5.937476 s

Results

genesymbolpredictionprobabilitymodelprediction
problem		splicingClinVaramino acid changesvariant typedbSNP IDprotein lengthfile
BCS1Ldisease_causing0.999999999986339simple_aaeaffectedR184Csingle base exchangers121908578show file
BCS1Ldisease_causing0.999999999986339simple_aaeaffectedR184Csingle base exchangers121908578show file
BCS1Ldisease_causing0.999999999986339simple_aaeaffectedR184Csingle base exchangers121908578show file
BCS1Ldisease_causing0.999999999986339simple_aaeaffectedR184Csingle base exchangers121908578show file
BCS1Ldisease_causing0.999999999986339simple_aaeaffectedR184Csingle base exchangers121908578show file
BCS1Ldisease_causing0.999999999986339simple_aaeaffectedR184Csingle base exchangers121908578show file
BCS1Ldisease_causing0.999999999986339simple_aaeaffectedR184Csingle base exchangers121908578show file

Taster files

Yum, tasty mutations...

mutation t@sting

 documentation

Prediction

disease causing

 Model: simple_aae, prob: 0.999999999986339      (explain)
Summary
  • amino acid sequence changed
  • known as potential disease variant: rs6171 (probable pathogenic)
  • known disease mutation at this position (HGMD CM070649)
  • protein features (might be) affected
  • splice site changes
 hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr2:219526571C>TN/A show variant in all transcripts   IGV
HGNC symbol BCS1L
Ensembl transcript ID ENST00000359273
Genbank transcript ID NM_001079866
UniProt peptide Q9Y276
alteration type single base exchange
alteration region CDS
DNA changes c.550C>T
cDNA.687C>T
g.3085C>T
AA changes R184C Score: 180 explain score(s)
position(s) of altered AA
if AA alteration in CDS		 184
frameshift no
known variant Reference ID: rs121908578
databasehomozygous (T/T)heterozygousallele carriers
1000G---
ExAC11819

known as potential disease variant: rs6171 (probable pathogenic for Mitochondrial complex III deficiency, nuclear type 1|Leigh syndrome|GRACILE syndrome|Bjornstad syndrome with mild mitochondrial complex III deficiency|not provided) dbSNP  NCBI variation viewer
known disease mutation at this position, please check HGMD for details (HGMD ID CM070649)

known disease mutation at this position, please check HGMD for details (HGMD ID CM070649)
known disease mutation at this position, please check HGMD for details (HGMD ID CM070649)
regulatory features H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)0.1150.994
4.441
(flanking)4.6151
explain score(s) and/or inspect your position(s) in in UCSC Genome Browser
splice sites
effectgDNA positionscorewt detection sequence exon-intron border
Acc increased3089wt: 0.42 / mu: 0.52wt: CTTTGGCTATCCACGCCGCCGGCGACCACTGAATTCTGTGG
mu: CTTTGGCTATCCACGCTGCCGGCGACCACTGAATTCTGTGG		 gccg|GCGA
Donor gained30890.51mu: CTGCCGGCGACCACT GCCG|gcga
distance from splice site 90
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      184GSEWRPFGYPRRRRPLNSVVLQQG
mutated  not conserved    184YPRCRRPLNSVVLQQ
Ptroglodytes  no homologue    
Mmulatta  all identical  ENSMMUG00000006740  184YPRRRRPLNSVVLQQ
Fcatus  no homologue    
Mmusculus  all identical  ENSMUSG00000026172  184YPRRRRPLDSVVLQQ
Ggallus  all identical  ENSGALG00000011386  184FPRRRRPLSSVVLEK
Trubripes  all identical  ENSTRUG00000006343  184FPRRRRPLSSVVLEA
Drerio  all identical  ENSDARG00000012295  184FPRRRRPLSSVVLES
Dmelanogaster  all identical  FBgn0032195  185GHPRRRRPTGSVVLDR
Celegans  all conserved  F54C9.6  204PRKKRDIESVILDG
Xtropicalis  all identical  ENSXETG00000013844  184FPRRRRPLSSVVLEE
protein features
start (aa)end (aa)featuredetails 
33419TOPO_DOMMitochondrial matrix (Potential).lost
230237NP_BINDATP (Potential).might get lost (downstream of altered splice site)
394394CONFLICTA -> T (in Ref. 6; CAE11877).might get lost (downstream of altered splice site)
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 1260 / 1260
position (AA) of stopcodon in wt / mu AA sequence 420 / 420
position of stopcodon in wt / mu cDNA 1397 / 1397
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 138 / 138
chromosome 2
strand 1
last intron/exon boundary 1145
theoretical NMD boundary in CDS 957
length of CDS 1260
coding sequence (CDS) position 550
cDNA position
(for ins/del: last normal base / first normal base)		 687
gDNA position
(for ins/del: last normal base / first normal base)		 3085
chromosomal position
(for ins/del: last normal base / first normal base)		 219526571
original gDNA sequence snippet GTCCCTTTGGCTATCCACGCCGCCGGCGACCACTGAATTCT
altered gDNA sequence snippet GTCCCTTTGGCTATCCACGCTGCCGGCGACCACTGAATTCT
original cDNA sequence snippet GTCCCTTTGGCTATCCACGCCGCCGGCGACCACTGAATTCT
altered cDNA sequence snippet GTCCCTTTGGCTATCCACGCTGCCGGCGACCACTGAATTCT
wildtype AA sequence MPLSDFILAL KDNPYFGAGF GLVGVGTALA LARKGVQLGL VAFRRHYMIT LEVPARDRSY
AWLLSWLTRH STRTQHLSVE TSYLQHESGR ISTKFEFVPS PGNHFIWYRG KWIRVERSRE
MQMIDLQTGT PWESVTFTAL GTDRKVFFNI LEEARELALQ QEEGKTVMYT AVGSEWRPFG
YPRRRRPLNS VVLQQGLADR IVRDVQEFID NPKWYTDRGI PYRRGYLLYG PPGCGKSSFI
TALAGELEHS ICLLSLTDSS LSDDRLNHLL SVAPQQSLVL LEDVDAAFLS RDLAVENPVK
YQGLGRLTFS GLLNALDGVA STEARIVFMT TNHVDRLDPA LIRPGRVDLK EYVGYCSHWQ
LTQMFQRFYP GQAPSLAENF AEHVLRATNQ ISPAQVQGYF MLYKNDPVGA IHNAESLRR*
mutated AA sequence MPLSDFILAL KDNPYFGAGF GLVGVGTALA LARKGVQLGL VAFRRHYMIT LEVPARDRSY
AWLLSWLTRH STRTQHLSVE TSYLQHESGR ISTKFEFVPS PGNHFIWYRG KWIRVERSRE
MQMIDLQTGT PWESVTFTAL GTDRKVFFNI LEEARELALQ QEEGKTVMYT AVGSEWRPFG
YPRCRRPLNS VVLQQGLADR IVRDVQEFID NPKWYTDRGI PYRRGYLLYG PPGCGKSSFI
TALAGELEHS ICLLSLTDSS LSDDRLNHLL SVAPQQSLVL LEDVDAAFLS RDLAVENPVK
YQGLGRLTFS GLLNALDGVA STEARIVFMT TNHVDRLDPA LIRPGRVDLK EYVGYCSHWQ
LTQMFQRFYP GQAPSLAENF AEHVLRATNQ ISPAQVQGYF MLYKNDPVGA IHNAESLRR*
speed 0.80 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: 0.999999999986339      (explain)
Summary
  • amino acid sequence changed
  • known as potential disease variant: rs6171 (probable pathogenic)
  • known disease mutation at this position (HGMD CM070649)
  • protein features (might be) affected
  • splice site changes
 hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr2:219526571C>TN/A show variant in all transcripts   IGV
HGNC symbol BCS1L
Ensembl transcript ID ENST00000392109
Genbank transcript ID NM_001257343
UniProt peptide Q9Y276
alteration type single base exchange
alteration region CDS
DNA changes c.550C>T
cDNA.816C>T
g.3085C>T
AA changes R184C Score: 180 explain score(s)
position(s) of altered AA
if AA alteration in CDS		 184
frameshift no
known variant Reference ID: rs121908578
databasehomozygous (T/T)heterozygousallele carriers
1000G---
ExAC11819

known as potential disease variant: rs6171 (probable pathogenic for Mitochondrial complex III deficiency, nuclear type 1|Leigh syndrome|GRACILE syndrome|Bjornstad syndrome with mild mitochondrial complex III deficiency|not provided) dbSNP  NCBI variation viewer
known disease mutation at this position, please check HGMD for details (HGMD ID CM070649)

known disease mutation at this position, please check HGMD for details (HGMD ID CM070649)
known disease mutation at this position, please check HGMD for details (HGMD ID CM070649)
regulatory features H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)0.1150.994
4.441
(flanking)4.6151
explain score(s) and/or inspect your position(s) in in UCSC Genome Browser
splice sites
effectgDNA positionscorewt detection sequence exon-intron border
Acc increased3089wt: 0.42 / mu: 0.52wt: CTTTGGCTATCCACGCCGCCGGCGACCACTGAATTCTGTGG
mu: CTTTGGCTATCCACGCTGCCGGCGACCACTGAATTCTGTGG		 gccg|GCGA
Donor gained30890.51mu: CTGCCGGCGACCACT GCCG|gcga
distance from splice site 90
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      184GSEWRPFGYPRRRRPLNSVVLQQG
mutated  not conserved    184YPRCRRPLNSVVLQQ
Ptroglodytes  no homologue    
Mmulatta  all identical  ENSMMUG00000006740  184YPRRRRPLNSVVLQQ
Fcatus  no homologue    
Mmusculus  all identical  ENSMUSG00000026172  184YPRRRRPLDSVVLQQ
Ggallus  all identical  ENSGALG00000011386  184FPRRRRPLSSVVLEK
Trubripes  all identical  ENSTRUG00000006343  184FPRRRRPLSSVVLEA
Drerio  all identical  ENSDARG00000012295  184FPRRRRPLSSVVLES
Dmelanogaster  all identical  FBgn0032195  185GHPRRRRPTGSVVLDR
Celegans  all conserved  F54C9.6  204PRKKRDIESVILDG
Xtropicalis  all identical  ENSXETG00000013844  184FPRRRRPLSSVVLEE
protein features
start (aa)end (aa)featuredetails 
33419TOPO_DOMMitochondrial matrix (Potential).lost
230237NP_BINDATP (Potential).might get lost (downstream of altered splice site)
394394CONFLICTA -> T (in Ref. 6; CAE11877).might get lost (downstream of altered splice site)
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 1260 / 1260
position (AA) of stopcodon in wt / mu AA sequence 420 / 420
position of stopcodon in wt / mu cDNA 1526 / 1526
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 267 / 267
chromosome 2
strand 1
last intron/exon boundary 1274
theoretical NMD boundary in CDS 957
length of CDS 1260
coding sequence (CDS) position 550
cDNA position
(for ins/del: last normal base / first normal base)		 816
gDNA position
(for ins/del: last normal base / first normal base)		 3085
chromosomal position
(for ins/del: last normal base / first normal base)		 219526571
original gDNA sequence snippet GTCCCTTTGGCTATCCACGCCGCCGGCGACCACTGAATTCT
altered gDNA sequence snippet GTCCCTTTGGCTATCCACGCTGCCGGCGACCACTGAATTCT
original cDNA sequence snippet GTCCCTTTGGCTATCCACGCCGCCGGCGACCACTGAATTCT
altered cDNA sequence snippet GTCCCTTTGGCTATCCACGCTGCCGGCGACCACTGAATTCT
wildtype AA sequence MPLSDFILAL KDNPYFGAGF GLVGVGTALA LARKGVQLGL VAFRRHYMIT LEVPARDRSY
AWLLSWLTRH STRTQHLSVE TSYLQHESGR ISTKFEFVPS PGNHFIWYRG KWIRVERSRE
MQMIDLQTGT PWESVTFTAL GTDRKVFFNI LEEARELALQ QEEGKTVMYT AVGSEWRPFG
YPRRRRPLNS VVLQQGLADR IVRDVQEFID NPKWYTDRGI PYRRGYLLYG PPGCGKSSFI
TALAGELEHS ICLLSLTDSS LSDDRLNHLL SVAPQQSLVL LEDVDAAFLS RDLAVENPVK
YQGLGRLTFS GLLNALDGVA STEARIVFMT TNHVDRLDPA LIRPGRVDLK EYVGYCSHWQ
LTQMFQRFYP GQAPSLAENF AEHVLRATNQ ISPAQVQGYF MLYKNDPVGA IHNAESLRR*
mutated AA sequence MPLSDFILAL KDNPYFGAGF GLVGVGTALA LARKGVQLGL VAFRRHYMIT LEVPARDRSY
AWLLSWLTRH STRTQHLSVE TSYLQHESGR ISTKFEFVPS PGNHFIWYRG KWIRVERSRE
MQMIDLQTGT PWESVTFTAL GTDRKVFFNI LEEARELALQ QEEGKTVMYT AVGSEWRPFG
YPRCRRPLNS VVLQQGLADR IVRDVQEFID NPKWYTDRGI PYRRGYLLYG PPGCGKSSFI
TALAGELEHS ICLLSLTDSS LSDDRLNHLL SVAPQQSLVL LEDVDAAFLS RDLAVENPVK
YQGLGRLTFS GLLNALDGVA STEARIVFMT TNHVDRLDPA LIRPGRVDLK EYVGYCSHWQ
LTQMFQRFYP GQAPSLAENF AEHVLRATNQ ISPAQVQGYF MLYKNDPVGA IHNAESLRR*
speed 0.95 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: 0.999999999986339      (explain)
Summary
  • amino acid sequence changed
  • known as potential disease variant: rs6171 (probable pathogenic)
  • known disease mutation at this position (HGMD CM070649)
  • protein features (might be) affected
  • splice site changes
 hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr2:219526571C>TN/A show variant in all transcripts   IGV
HGNC symbol BCS1L
Ensembl transcript ID ENST00000392110
Genbank transcript ID NM_001257342
UniProt peptide Q9Y276
alteration type single base exchange
alteration region CDS
DNA changes c.550C>T
cDNA.759C>T
g.3085C>T
AA changes R184C Score: 180 explain score(s)
position(s) of altered AA
if AA alteration in CDS		 184
frameshift no
known variant Reference ID: rs121908578
databasehomozygous (T/T)heterozygousallele carriers
1000G---
ExAC11819

known as potential disease variant: rs6171 (probable pathogenic for Mitochondrial complex III deficiency, nuclear type 1|Leigh syndrome|GRACILE syndrome|Bjornstad syndrome with mild mitochondrial complex III deficiency|not provided) dbSNP  NCBI variation viewer
known disease mutation at this position, please check HGMD for details (HGMD ID CM070649)

known disease mutation at this position, please check HGMD for details (HGMD ID CM070649)
known disease mutation at this position, please check HGMD for details (HGMD ID CM070649)
regulatory features H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)0.1150.994
4.441
(flanking)4.6151
explain score(s) and/or inspect your position(s) in in UCSC Genome Browser
splice sites
effectgDNA positionscorewt detection sequence exon-intron border
Acc increased3089wt: 0.42 / mu: 0.52wt: CTTTGGCTATCCACGCCGCCGGCGACCACTGAATTCTGTGG
mu: CTTTGGCTATCCACGCTGCCGGCGACCACTGAATTCTGTGG		 gccg|GCGA
Donor gained30890.51mu: CTGCCGGCGACCACT GCCG|gcga
distance from splice site 90
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      184GSEWRPFGYPRRRRPLNSVVLQQG
mutated  not conserved    184YPRCRRPLNSVVLQQ
Ptroglodytes  no homologue    
Mmulatta  all identical  ENSMMUG00000006740  184YPRRRRPLNSVVLQQ
Fcatus  no homologue    
Mmusculus  all identical  ENSMUSG00000026172  184YPRRRRPLDSVVLQQ
Ggallus  all identical  ENSGALG00000011386  184FPRRRRPLSSVVLEK
Trubripes  all identical  ENSTRUG00000006343  184FPRRRRPLSSVVLEA
Drerio  all identical  ENSDARG00000012295  184FPRRRRPLSSVVLES
Dmelanogaster  all identical  FBgn0032195  185GHPRRRRPTGSVVLDR
Celegans  all conserved  F54C9.6  204PRKKRDIESVILDG
Xtropicalis  all identical  ENSXETG00000013844  184FPRRRRPLSSVVLEE
protein features
start (aa)end (aa)featuredetails 
33419TOPO_DOMMitochondrial matrix (Potential).lost
230237NP_BINDATP (Potential).might get lost (downstream of altered splice site)
394394CONFLICTA -> T (in Ref. 6; CAE11877).might get lost (downstream of altered splice site)
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 1260 / 1260
position (AA) of stopcodon in wt / mu AA sequence 420 / 420
position of stopcodon in wt / mu cDNA 1469 / 1469
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 210 / 210
chromosome 2
strand 1
last intron/exon boundary 1217
theoretical NMD boundary in CDS 957
length of CDS 1260
coding sequence (CDS) position 550
cDNA position
(for ins/del: last normal base / first normal base)		 759
gDNA position
(for ins/del: last normal base / first normal base)		 3085
chromosomal position
(for ins/del: last normal base / first normal base)		 219526571
original gDNA sequence snippet GTCCCTTTGGCTATCCACGCCGCCGGCGACCACTGAATTCT
altered gDNA sequence snippet GTCCCTTTGGCTATCCACGCTGCCGGCGACCACTGAATTCT
original cDNA sequence snippet GTCCCTTTGGCTATCCACGCCGCCGGCGACCACTGAATTCT
altered cDNA sequence snippet GTCCCTTTGGCTATCCACGCTGCCGGCGACCACTGAATTCT
wildtype AA sequence MPLSDFILAL KDNPYFGAGF GLVGVGTALA LARKGVQLGL VAFRRHYMIT LEVPARDRSY
AWLLSWLTRH STRTQHLSVE TSYLQHESGR ISTKFEFVPS PGNHFIWYRG KWIRVERSRE
MQMIDLQTGT PWESVTFTAL GTDRKVFFNI LEEARELALQ QEEGKTVMYT AVGSEWRPFG
YPRRRRPLNS VVLQQGLADR IVRDVQEFID NPKWYTDRGI PYRRGYLLYG PPGCGKSSFI
TALAGELEHS ICLLSLTDSS LSDDRLNHLL SVAPQQSLVL LEDVDAAFLS RDLAVENPVK
YQGLGRLTFS GLLNALDGVA STEARIVFMT TNHVDRLDPA LIRPGRVDLK EYVGYCSHWQ
LTQMFQRFYP GQAPSLAENF AEHVLRATNQ ISPAQVQGYF MLYKNDPVGA IHNAESLRR*
mutated AA sequence MPLSDFILAL KDNPYFGAGF GLVGVGTALA LARKGVQLGL VAFRRHYMIT LEVPARDRSY
AWLLSWLTRH STRTQHLSVE TSYLQHESGR ISTKFEFVPS PGNHFIWYRG KWIRVERSRE
MQMIDLQTGT PWESVTFTAL GTDRKVFFNI LEEARELALQ QEEGKTVMYT AVGSEWRPFG
YPRCRRPLNS VVLQQGLADR IVRDVQEFID NPKWYTDRGI PYRRGYLLYG PPGCGKSSFI
TALAGELEHS ICLLSLTDSS LSDDRLNHLL SVAPQQSLVL LEDVDAAFLS RDLAVENPVK
YQGLGRLTFS GLLNALDGVA STEARIVFMT TNHVDRLDPA LIRPGRVDLK EYVGYCSHWQ
LTQMFQRFYP GQAPSLAENF AEHVLRATNQ ISPAQVQGYF MLYKNDPVGA IHNAESLRR*
speed 0.63 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: 0.999999999986339      (explain)
Summary
  • amino acid sequence changed
  • known as potential disease variant: rs6171 (probable pathogenic)
  • known disease mutation at this position (HGMD CM070649)
  • protein features (might be) affected
  • splice site changes
 hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr2:219526571C>TN/A show variant in all transcripts   IGV
HGNC symbol BCS1L
Ensembl transcript ID ENST00000392111
Genbank transcript ID NM_004328
UniProt peptide Q9Y276
alteration type single base exchange
alteration region CDS
DNA changes c.550C>T
cDNA.817C>T
g.3085C>T
AA changes R184C Score: 180 explain score(s)
position(s) of altered AA
if AA alteration in CDS		 184
frameshift no
known variant Reference ID: rs121908578
databasehomozygous (T/T)heterozygousallele carriers
1000G---
ExAC11819

known as potential disease variant: rs6171 (probable pathogenic for Mitochondrial complex III deficiency, nuclear type 1|Leigh syndrome|GRACILE syndrome|Bjornstad syndrome with mild mitochondrial complex III deficiency|not provided) dbSNP  NCBI variation viewer
known disease mutation at this position, please check HGMD for details (HGMD ID CM070649)

known disease mutation at this position, please check HGMD for details (HGMD ID CM070649)
known disease mutation at this position, please check HGMD for details (HGMD ID CM070649)
regulatory features H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)0.1150.994
4.441
(flanking)4.6151
explain score(s) and/or inspect your position(s) in in UCSC Genome Browser
splice sites
effectgDNA positionscorewt detection sequence exon-intron border
Acc increased3089wt: 0.42 / mu: 0.52wt: CTTTGGCTATCCACGCCGCCGGCGACCACTGAATTCTGTGG
mu: CTTTGGCTATCCACGCTGCCGGCGACCACTGAATTCTGTGG		 gccg|GCGA
Donor gained30890.51mu: CTGCCGGCGACCACT GCCG|gcga
distance from splice site 90
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      184GSEWRPFGYPRRRRPLNSVVLQQG
mutated  not conserved    184YPRCRRPLNSVVLQQ
Ptroglodytes  no homologue    
Mmulatta  all identical  ENSMMUG00000006740  184YPRRRRPLNSVVLQQ
Fcatus  no homologue    
Mmusculus  all identical  ENSMUSG00000026172  184YPRRRRPLDSVVLQQ
Ggallus  all identical  ENSGALG00000011386  184FPRRRRPLSSVVLEK
Trubripes  all identical  ENSTRUG00000006343  184FPRRRRPLSSVVLEA
Drerio  all identical  ENSDARG00000012295  184FPRRRRPLSSVVLES
Dmelanogaster  all identical  FBgn0032195  185GHPRRRRPTGSVVLDR
Celegans  all conserved  F54C9.6  204PRKKRDIESVILDG
Xtropicalis  all identical  ENSXETG00000013844  184FPRRRRPLSSVVLEE
protein features
start (aa)end (aa)featuredetails 
33419TOPO_DOMMitochondrial matrix (Potential).lost
230237NP_BINDATP (Potential).might get lost (downstream of altered splice site)
394394CONFLICTA -> T (in Ref. 6; CAE11877).might get lost (downstream of altered splice site)
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 1260 / 1260
position (AA) of stopcodon in wt / mu AA sequence 420 / 420
position of stopcodon in wt / mu cDNA 1527 / 1527
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 268 / 268
chromosome 2
strand 1
last intron/exon boundary 1275
theoretical NMD boundary in CDS 957
length of CDS 1260
coding sequence (CDS) position 550
cDNA position
(for ins/del: last normal base / first normal base)		 817
gDNA position
(for ins/del: last normal base / first normal base)		 3085
chromosomal position
(for ins/del: last normal base / first normal base)		 219526571
original gDNA sequence snippet GTCCCTTTGGCTATCCACGCCGCCGGCGACCACTGAATTCT
altered gDNA sequence snippet GTCCCTTTGGCTATCCACGCTGCCGGCGACCACTGAATTCT
original cDNA sequence snippet GTCCCTTTGGCTATCCACGCCGCCGGCGACCACTGAATTCT
altered cDNA sequence snippet GTCCCTTTGGCTATCCACGCTGCCGGCGACCACTGAATTCT
wildtype AA sequence MPLSDFILAL KDNPYFGAGF GLVGVGTALA LARKGVQLGL VAFRRHYMIT LEVPARDRSY
AWLLSWLTRH STRTQHLSVE TSYLQHESGR ISTKFEFVPS PGNHFIWYRG KWIRVERSRE
MQMIDLQTGT PWESVTFTAL GTDRKVFFNI LEEARELALQ QEEGKTVMYT AVGSEWRPFG
YPRRRRPLNS VVLQQGLADR IVRDVQEFID NPKWYTDRGI PYRRGYLLYG PPGCGKSSFI
TALAGELEHS ICLLSLTDSS LSDDRLNHLL SVAPQQSLVL LEDVDAAFLS RDLAVENPVK
YQGLGRLTFS GLLNALDGVA STEARIVFMT TNHVDRLDPA LIRPGRVDLK EYVGYCSHWQ
LTQMFQRFYP GQAPSLAENF AEHVLRATNQ ISPAQVQGYF MLYKNDPVGA IHNAESLRR*
mutated AA sequence MPLSDFILAL KDNPYFGAGF GLVGVGTALA LARKGVQLGL VAFRRHYMIT LEVPARDRSY
AWLLSWLTRH STRTQHLSVE TSYLQHESGR ISTKFEFVPS PGNHFIWYRG KWIRVERSRE
MQMIDLQTGT PWESVTFTAL GTDRKVFFNI LEEARELALQ QEEGKTVMYT AVGSEWRPFG
YPRCRRPLNS VVLQQGLADR IVRDVQEFID NPKWYTDRGI PYRRGYLLYG PPGCGKSSFI
TALAGELEHS ICLLSLTDSS LSDDRLNHLL SVAPQQSLVL LEDVDAAFLS RDLAVENPVK
YQGLGRLTFS GLLNALDGVA STEARIVFMT TNHVDRLDPA LIRPGRVDLK EYVGYCSHWQ
LTQMFQRFYP GQAPSLAENF AEHVLRATNQ ISPAQVQGYF MLYKNDPVGA IHNAESLRR*
speed 1.33 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: 0.999999999986339      (explain)
Summary
  • amino acid sequence changed
  • known as potential disease variant: rs6171 (probable pathogenic)
  • known disease mutation at this position (HGMD CM070649)
  • protein features (might be) affected
  • splice site changes
 hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr2:219526571C>TN/A show variant in all transcripts   IGV
HGNC symbol BCS1L
Ensembl transcript ID ENST00000412366
Genbank transcript ID NM_001257344
UniProt peptide Q9Y276
alteration type single base exchange
alteration region CDS
DNA changes c.550C>T
cDNA.663C>T
g.3085C>T
AA changes R184C Score: 180 explain score(s)
position(s) of altered AA
if AA alteration in CDS		 184
frameshift no
known variant Reference ID: rs121908578
databasehomozygous (T/T)heterozygousallele carriers
1000G---
ExAC11819

known as potential disease variant: rs6171 (probable pathogenic for Mitochondrial complex III deficiency, nuclear type 1|Leigh syndrome|GRACILE syndrome|Bjornstad syndrome with mild mitochondrial complex III deficiency|not provided) dbSNP  NCBI variation viewer
known disease mutation at this position, please check HGMD for details (HGMD ID CM070649)

known disease mutation at this position, please check HGMD for details (HGMD ID CM070649)
known disease mutation at this position, please check HGMD for details (HGMD ID CM070649)
regulatory features H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)0.1150.994
4.441
(flanking)4.6151
explain score(s) and/or inspect your position(s) in in UCSC Genome Browser
splice sites
effectgDNA positionscorewt detection sequence exon-intron border
Acc increased3089wt: 0.42 / mu: 0.52wt: CTTTGGCTATCCACGCCGCCGGCGACCACTGAATTCTGTGG
mu: CTTTGGCTATCCACGCTGCCGGCGACCACTGAATTCTGTGG		 gccg|GCGA
Donor gained30890.51mu: CTGCCGGCGACCACT GCCG|gcga
distance from splice site 90
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      184GSEWRPFGYPRRRRPLNSVVLQQG
mutated  not conserved    184YPRCRRPLNSVVLQQ
Ptroglodytes  no homologue    
Mmulatta  all identical  ENSMMUG00000006740  184YPRRRRPLNSVVLQQ
Fcatus  no homologue    
Mmusculus  all identical  ENSMUSG00000026172  184YPRRRRPLDSVVLQQ
Ggallus  all identical  ENSGALG00000011386  184FPRRRRPLSSVVLEK
Trubripes  all identical  ENSTRUG00000006343  184FPRRRRPLSSVVLEA
Drerio  all identical  ENSDARG00000012295  184FPRRRRPLSSVVLES
Dmelanogaster  all identical  FBgn0032195  185GHPRRRRPTGSVVLDR
Celegans  all conserved  F54C9.6  204PRKKRDIESVILDG
Xtropicalis  all identical  ENSXETG00000013844  184FPRRRRPLSSVVLEE
protein features
start (aa)end (aa)featuredetails 
33419TOPO_DOMMitochondrial matrix (Potential).lost
230237NP_BINDATP (Potential).might get lost (downstream of altered splice site)
394394CONFLICTA -> T (in Ref. 6; CAE11877).might get lost (downstream of altered splice site)
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 1260 / 1260
position (AA) of stopcodon in wt / mu AA sequence 420 / 420
position of stopcodon in wt / mu cDNA 1373 / 1373
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 114 / 114
chromosome 2
strand 1
last intron/exon boundary 1121
theoretical NMD boundary in CDS 957
length of CDS 1260
coding sequence (CDS) position 550
cDNA position
(for ins/del: last normal base / first normal base)		 663
gDNA position
(for ins/del: last normal base / first normal base)		 3085
chromosomal position
(for ins/del: last normal base / first normal base)		 219526571
original gDNA sequence snippet GTCCCTTTGGCTATCCACGCCGCCGGCGACCACTGAATTCT
altered gDNA sequence snippet GTCCCTTTGGCTATCCACGCTGCCGGCGACCACTGAATTCT
original cDNA sequence snippet GTCCCTTTGGCTATCCACGCCGCCGGCGACCACTGAATTCT
altered cDNA sequence snippet GTCCCTTTGGCTATCCACGCTGCCGGCGACCACTGAATTCT
wildtype AA sequence MPLSDFILAL KDNPYFGAGF GLVGVGTALA LARKGVQLGL VAFRRHYMIT LEVPARDRSY
AWLLSWLTRH STRTQHLSVE TSYLQHESGR ISTKFEFVPS PGNHFIWYRG KWIRVERSRE
MQMIDLQTGT PWESVTFTAL GTDRKVFFNI LEEARELALQ QEEGKTVMYT AVGSEWRPFG
YPRRRRPLNS VVLQQGLADR IVRDVQEFID NPKWYTDRGI PYRRGYLLYG PPGCGKSSFI
TALAGELEHS ICLLSLTDSS LSDDRLNHLL SVAPQQSLVL LEDVDAAFLS RDLAVENPVK
YQGLGRLTFS GLLNALDGVA STEARIVFMT TNHVDRLDPA LIRPGRVDLK EYVGYCSHWQ
LTQMFQRFYP GQAPSLAENF AEHVLRATNQ ISPAQVQGYF MLYKNDPVGA IHNAESLRR*
mutated AA sequence MPLSDFILAL KDNPYFGAGF GLVGVGTALA LARKGVQLGL VAFRRHYMIT LEVPARDRSY
AWLLSWLTRH STRTQHLSVE TSYLQHESGR ISTKFEFVPS PGNHFIWYRG KWIRVERSRE
MQMIDLQTGT PWESVTFTAL GTDRKVFFNI LEEARELALQ QEEGKTVMYT AVGSEWRPFG
YPRCRRPLNS VVLQQGLADR IVRDVQEFID NPKWYTDRGI PYRRGYLLYG PPGCGKSSFI
TALAGELEHS ICLLSLTDSS LSDDRLNHLL SVAPQQSLVL LEDVDAAFLS RDLAVENPVK
YQGLGRLTFS GLLNALDGVA STEARIVFMT TNHVDRLDPA LIRPGRVDLK EYVGYCSHWQ
LTQMFQRFYP GQAPSLAENF AEHVLRATNQ ISPAQVQGYF MLYKNDPVGA IHNAESLRR*
speed 0.63 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: 0.999999999986339      (explain)
Summary
  • amino acid sequence changed
  • known as potential disease variant: rs6171 (probable pathogenic)
  • known disease mutation at this position (HGMD CM070649)
  • protein features (might be) affected
  • splice site changes
 hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr2:219526571C>TN/A show variant in all transcripts   IGV
HGNC symbol BCS1L
Ensembl transcript ID ENST00000439945
Genbank transcript ID N/A
UniProt peptide Q9Y276
alteration type single base exchange
alteration region CDS
DNA changes c.550C>T
cDNA.755C>T
g.3085C>T
AA changes R184C Score: 180 explain score(s)
position(s) of altered AA
if AA alteration in CDS		 184
frameshift no
known variant Reference ID: rs121908578
databasehomozygous (T/T)heterozygousallele carriers
1000G---
ExAC11819

known as potential disease variant: rs6171 (probable pathogenic for Mitochondrial complex III deficiency, nuclear type 1|Leigh syndrome|GRACILE syndrome|Bjornstad syndrome with mild mitochondrial complex III deficiency|not provided) dbSNP  NCBI variation viewer
known disease mutation at this position, please check HGMD for details (HGMD ID CM070649)

known disease mutation at this position, please check HGMD for details (HGMD ID CM070649)
known disease mutation at this position, please check HGMD for details (HGMD ID CM070649)
regulatory features H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)0.1150.994
4.441
(flanking)4.6151
explain score(s) and/or inspect your position(s) in in UCSC Genome Browser
splice sites
effectgDNA positionscorewt detection sequence exon-intron border
Acc increased3089wt: 0.42 / mu: 0.52wt: CTTTGGCTATCCACGCCGCCGGCGACCACTGAATTCTGTGG
mu: CTTTGGCTATCCACGCTGCCGGCGACCACTGAATTCTGTGG		 gccg|GCGA
Donor gained30890.51mu: CTGCCGGCGACCACT GCCG|gcga
distance from splice site 90
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      184GSEWRPFGYPRRRRPLNSVVLQQG
mutated  not conserved    184YPRCRRPLNSVVLQQ
Ptroglodytes  no homologue    
Mmulatta  all identical  ENSMMUG00000006740  184YPRRRRPLNSVVLQQ
Fcatus  no homologue    
Mmusculus  all identical  ENSMUSG00000026172  184YPRRRRPLDSVVLQQ
Ggallus  all identical  ENSGALG00000011386  184FPRRRRPLSSVVLEK
Trubripes  all identical  ENSTRUG00000006343  184FPRRRRPLSSVVLEA
Drerio  all identical  ENSDARG00000012295  184FPRRRRPLSSVVLES
Dmelanogaster  all identical  FBgn0032195  185GHPRRRRPTGSVVLDR
Celegans  all conserved  F54C9.6  204PRKKRDIESVILDG
Xtropicalis  all identical  ENSXETG00000013844  184FPRRRRPLSSVVLEE
protein features
start (aa)end (aa)featuredetails 
33419TOPO_DOMMitochondrial matrix (Potential).lost
230237NP_BINDATP (Potential).might get lost (downstream of altered splice site)
394394CONFLICTA -> T (in Ref. 6; CAE11877).might get lost (downstream of altered splice site)
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 1260 / 1260
position (AA) of stopcodon in wt / mu AA sequence 420 / 420
position of stopcodon in wt / mu cDNA 1465 / 1465
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 206 / 206
chromosome 2
strand 1
last intron/exon boundary 1213
theoretical NMD boundary in CDS 957
length of CDS 1260
coding sequence (CDS) position 550
cDNA position
(for ins/del: last normal base / first normal base)		 755
gDNA position
(for ins/del: last normal base / first normal base)		 3085
chromosomal position
(for ins/del: last normal base / first normal base)		 219526571
original gDNA sequence snippet GTCCCTTTGGCTATCCACGCCGCCGGCGACCACTGAATTCT
altered gDNA sequence snippet GTCCCTTTGGCTATCCACGCTGCCGGCGACCACTGAATTCT
original cDNA sequence snippet GTCCCTTTGGCTATCCACGCCGCCGGCGACCACTGAATTCT
altered cDNA sequence snippet GTCCCTTTGGCTATCCACGCTGCCGGCGACCACTGAATTCT
wildtype AA sequence MPLSDFILAL KDNPYFGAGF GLVGVGTALA LARKGVQLGL VAFRRHYMIT LEVPARDRSY
AWLLSWLTRH STRTQHLSVE TSYLQHESGR ISTKFEFVPS PGNHFIWYRG KWIRVERSRE
MQMIDLQTGT PWESVTFTAL GTDRKVFFNI LEEARELALQ QEEGKTVMYT AVGSEWRPFG
YPRRRRPLNS VVLQQGLADR IVRDVQEFID NPKWYTDRGI PYRRGYLLYG PPGCGKSSFI
TALAGELEHS ICLLSLTDSS LSDDRLNHLL SVAPQQSLVL LEDVDAAFLS RDLAVENPVK
YQGLGRLTFS GLLNALDGVA STEARIVFMT TNHVDRLDPA LIRPGRVDLK EYVGYCSHWQ
LTQMFQRFYP GQAPSLAENF AEHVLRATNQ ISPAQVQGYF MLYKNDPVGA IHNAESLRR*
mutated AA sequence MPLSDFILAL KDNPYFGAGF GLVGVGTALA LARKGVQLGL VAFRRHYMIT LEVPARDRSY
AWLLSWLTRH STRTQHLSVE TSYLQHESGR ISTKFEFVPS PGNHFIWYRG KWIRVERSRE
MQMIDLQTGT PWESVTFTAL GTDRKVFFNI LEEARELALQ QEEGKTVMYT AVGSEWRPFG
YPRCRRPLNS VVLQQGLADR IVRDVQEFID NPKWYTDRGI PYRRGYLLYG PPGCGKSSFI
TALAGELEHS ICLLSLTDSS LSDDRLNHLL SVAPQQSLVL LEDVDAAFLS RDLAVENPVK
YQGLGRLTFS GLLNALDGVA STEARIVFMT TNHVDRLDPA LIRPGRVDLK EYVGYCSHWQ
LTQMFQRFYP GQAPSLAENF AEHVLRATNQ ISPAQVQGYF MLYKNDPVGA IHNAESLRR*
speed 0.56 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: 0.999999999986339      (explain)
Summary
  • amino acid sequence changed
  • known as potential disease variant: rs6171 (probable pathogenic)
  • known disease mutation at this position (HGMD CM070649)
  • protein features (might be) affected
  • splice site changes
 hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr2:219526571C>TN/A show variant in all transcripts   IGV
HGNC symbol BCS1L
Ensembl transcript ID ENST00000431802
Genbank transcript ID N/A
UniProt peptide Q9Y276
alteration type single base exchange
alteration region CDS
DNA changes c.550C>T
cDNA.1249C>T
g.3085C>T
AA changes R184C Score: 180 explain score(s)
position(s) of altered AA
if AA alteration in CDS		 184
frameshift no
known variant Reference ID: rs121908578
databasehomozygous (T/T)heterozygousallele carriers
1000G---
ExAC11819

known as potential disease variant: rs6171 (probable pathogenic for Mitochondrial complex III deficiency, nuclear type 1|Leigh syndrome|GRACILE syndrome|Bjornstad syndrome with mild mitochondrial complex III deficiency|not provided) dbSNP  NCBI variation viewer
known disease mutation at this position, please check HGMD for details (HGMD ID CM070649)

known disease mutation at this position, please check HGMD for details (HGMD ID CM070649)
known disease mutation at this position, please check HGMD for details (HGMD ID CM070649)
regulatory features H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)0.1150.994
4.441
(flanking)4.6151
explain score(s) and/or inspect your position(s) in in UCSC Genome Browser
splice sites
effectgDNA positionscorewt detection sequence exon-intron border
Acc increased3089wt: 0.42 / mu: 0.52wt: CTTTGGCTATCCACGCCGCCGGCGACCACTGAATTCTGTGG
mu: CTTTGGCTATCCACGCTGCCGGCGACCACTGAATTCTGTGG		 gccg|GCGA
Donor gained30890.51mu: CTGCCGGCGACCACT GCCG|gcga
distance from splice site 90
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      184GSEWRPFGYPRRRRPLNSVVLQQG
mutated  not conserved    184YPRCRRPLNSVVLQQ
Ptroglodytes  no homologue    
Mmulatta  all identical  ENSMMUG00000006740  184YPRRRRPLNSVVLQQ
Fcatus  no homologue    
Mmusculus  all identical  ENSMUSG00000026172  184YPRRRRPLDSVVLQQ
Ggallus  all identical  ENSGALG00000011386  184FPRRRRPLSSVVLEK
Trubripes  all identical  ENSTRUG00000006343  184FPRRRRPLSSVVLEA
Drerio  all identical  ENSDARG00000012295  184FPRRRRPLSSVVLES
Dmelanogaster  all identical  FBgn0032195  185GHPRRRRPTGSVVLDR
Celegans  all conserved  F54C9.6  204PRKKRDIESVILDG
Xtropicalis  all identical  ENSXETG00000013844  184FPRRRRPLSSVVLEE
protein features
start (aa)end (aa)featuredetails 
33419TOPO_DOMMitochondrial matrix (Potential).lost
230237NP_BINDATP (Potential).might get lost (downstream of altered splice site)
394394CONFLICTA -> T (in Ref. 6; CAE11877).might get lost (downstream of altered splice site)
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 1260 / 1260
position (AA) of stopcodon in wt / mu AA sequence 420 / 420
position of stopcodon in wt / mu cDNA 1959 / 1959
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 700 / 700
chromosome 2
strand 1
last intron/exon boundary 1707
theoretical NMD boundary in CDS 957
length of CDS 1260
coding sequence (CDS) position 550
cDNA position
(for ins/del: last normal base / first normal base)		 1249
gDNA position
(for ins/del: last normal base / first normal base)		 3085
chromosomal position
(for ins/del: last normal base / first normal base)		 219526571
original gDNA sequence snippet GTCCCTTTGGCTATCCACGCCGCCGGCGACCACTGAATTCT
altered gDNA sequence snippet GTCCCTTTGGCTATCCACGCTGCCGGCGACCACTGAATTCT
original cDNA sequence snippet GTCCCTTTGGCTATCCACGCCGCCGGCGACCACTGAATTCT
altered cDNA sequence snippet GTCCCTTTGGCTATCCACGCTGCCGGCGACCACTGAATTCT
wildtype AA sequence MPLSDFILAL KDNPYFGAGF GLVGVGTALA LARKGVQLGL VAFRRHYMIT LEVPARDRSY
AWLLSWLTRH STRTQHLSVE TSYLQHESGR ISTKFEFVPS PGNHFIWYRG KWIRVERSRE
MQMIDLQTGT PWESVTFTAL GTDRKVFFNI LEEARELALQ QEEGKTVMYT AVGSEWRPFG
YPRRRRPLNS VVLQQGLADR IVRDVQEFID NPKWYTDRGI PYRRGYLLYG PPGCGKSSFI
TALAGELEHS ICLLSLTDSS LSDDRLNHLL SVAPQQSLVL LEDVDAAFLS RDLAVENPVK
YQGLGRLTFS GLLNALDGVA STEARIVFMT TNHVDRLDPA LIRPGRVDLK EYVGYCSHWQ
LTQMFQRFYP GQAPSLAENF AEHVLRATNQ ISPAQVQGYF MLYKNDPVGA IHNAESLRR*
mutated AA sequence MPLSDFILAL KDNPYFGAGF GLVGVGTALA LARKGVQLGL VAFRRHYMIT LEVPARDRSY
AWLLSWLTRH STRTQHLSVE TSYLQHESGR ISTKFEFVPS PGNHFIWYRG KWIRVERSRE
MQMIDLQTGT PWESVTFTAL GTDRKVFFNI LEEARELALQ QEEGKTVMYT AVGSEWRPFG
YPRCRRPLNS VVLQQGLADR IVRDVQEFID NPKWYTDRGI PYRRGYLLYG PPGCGKSSFI
TALAGELEHS ICLLSLTDSS LSDDRLNHLL SVAPQQSLVL LEDVDAAFLS RDLAVENPVK
YQGLGRLTFS GLLNALDGVA STEARIVFMT TNHVDRLDPA LIRPGRVDLK EYVGYCSHWQ
LTQMFQRFYP GQAPSLAENF AEHVLRATNQ ISPAQVQGYF MLYKNDPVGA IHNAESLRR*
speed 0.82 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