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 4 transcript(s)...
Querying Taster for transcript #1: ENST00000540367
Querying Taster for transcript #2: ENST00000539743
Querying Taster for transcript #3: ENST00000376618
Querying Taster for transcript #4: ENST00000265641
MT speed 0 s - this script 4.387967 s

Results


genesymbolpredictionprobabilitymodelprediction
problem
splicingClinVaramino acid changesvariant typedbSNP IDprotein lengthfile
CPT1Adisease_causing_automatic0.999999999996992simple_aae0P479Lsingle base exchangers80356779show file
CPT1Adisease_causing_automatic0.999999999996992simple_aae0P479Lsingle base exchangers80356779show file
CPT1Adisease_causing_automatic0.999999999996992simple_aae0P479Lsingle base exchangers80356779show file
CPT1Adisease_causing_automatic0.999999999996992simple_aae0P479Lsingle base exchangers80356779show file

Taster files

Yum, tasty mutations...

mutation t@sting

documentation

Prediction

disease causing

Model: simple_aae, prob: 0.999999999996992 (classification due to ClinVar, real probability is shown anyway)      (explain)
Summary
  • amino acid sequence changed
  • known disease mutation at this position (HGMD CM016082)
  • known disease mutation: rs65644 (pathogenic)
  • protein features (might be) affected
hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr11:68548130G>AN/A show variant in all transcripts   IGV
HGNC symbol CPT1A
Ensembl transcript ID ENST00000540367
Genbank transcript ID N/A
UniProt peptide P50416
alteration type single base exchange
alteration region CDS
DNA changes c.1436C>T
cDNA.1465C>T
g.63749C>T
AA changes P479L Score: 98 explain score(s)
position(s) of altered AA
if AA alteration in CDS
479
frameshift no
known variant Reference ID: rs80356779
databasehomozygous (A/A)heterozygousallele carriers
1000G---
ExAC022

known disease mutation: rs65644 (pathogenic for CARNITINE PALMITOYLTRANSFERASE IA POLYMORPHISM|CPT1A ARCTIC VARIANT|Carnitine palmitoyltransferase type I deficiency|Carnitine palmitoyltransferase 1A deficiency|not provided) dbSNP  NCBI variation viewer
known disease mutation at this position, please check HGMD for details (HGMD ID CM016082)

known disease mutation at this position, please check HGMD for details (HGMD ID CM016082)
known disease mutation at this position, please check HGMD for details (HGMD ID CM016082)
regulatory features H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
H3K4me1, Histone, Histone 3 Lysine 4 Mono-Methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)-0.6690.75
6.0731
(flanking)6.0731
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 23
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      479GLNAEHSWADAPIVAHLWEYVMSI
mutated  not conserved    479GLNAEHSWADALIVAHLWEYVMS
Ptroglodytes  all identical  ENSPTRG00000003987  479GLNAEHSWADAPIVAHLWEYVMS
Mmulatta  all identical  ENSMMUG00000001780  479GINAEHSWADAPIMAHLWEYVMS
Fcatus  no homologue    
Mmusculus  all identical  ENSMUSG00000024900  479GINAEHSWADAPIVGHLWEYVMA
Ggallus  all identical  ENSGALG00000007077  479GLNAEHSWADAPIVGHLWENVMA
Trubripes  all identical  ENSTRUG00000009681  482APIVGHLWEHVLS
Drerio  all identical  ENSDARG00000062054  479GLNAEHSWADAPIVGHLWEQVLS
Dmelanogaster  not conserved  FBgn0261862  477TWSDAAIASHMWENLIV
Celegans  not conserved  Y46G5A.17  480AVMAHFTEWSLL
Xtropicalis  no homologue    
protein features
start (aa)end (aa)featuredetails 
123773TOPO_DOMCytoplasmic (Potential).lost
479479CONFLICTP -> Q (in Ref. 1; AAC41748).lost
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 2271 / 2271
position (AA) of stopcodon in wt / mu AA sequence 757 / 757
position of stopcodon in wt / mu cDNA 2300 / 2300
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 30 / 30
chromosome 11
strand -1
last intron/exon boundary 2265
theoretical NMD boundary in CDS 2185
length of CDS 2271
coding sequence (CDS) position 1436
cDNA position
(for ins/del: last normal base / first normal base)
1465
gDNA position
(for ins/del: last normal base / first normal base)
63749
chromosomal position
(for ins/del: last normal base / first normal base)
68548130
original gDNA sequence snippet ACACTCCTGGGCAGATGCGCCGATCGTGGCCCACCTTTGGG
altered gDNA sequence snippet ACACTCCTGGGCAGATGCGCTGATCGTGGCCCACCTTTGGG
original cDNA sequence snippet ACACTCCTGGGCAGATGCGCCGATCGTGGCCCACCTTTGGG
altered cDNA sequence snippet ACACTCCTGGGCAGATGCGCTGATCGTGGCCCACCTTTGGG
wildtype AA sequence MAEAHQAVAF QFTVTPDGID LRLSHEALRQ IYLSGLHSWK KKFIRFKNGI ITGVYPASPS
SWLIVVVGVM TTMYAKIDPS LGIIAKINRT LETANCMSSQ TKNVVSGVLF GTGLWVALIV
TMRYSLKVLL SYHGWMFTEH GKMSRATKIW MGMVKIFSGR KPMLYSFQTS LPRLPVPAVK
DTVNRYLQSV RPLMKEEDFK RMTALAQDFA VGLGPRLQWY LKLKSWWATN YVSDWWEEYI
YLRGRGPLMV NSNYYAMDLL YILPTHIQAA RAGNAIHAIL LYRRKLDREE IKPIRLLGST
IPLCSAQWER MFNTSRIPGE ETDTIQHMRD SKHIVVYHRG RYFKVWLYHD GRLLKPREME
QQMQRILDNT SEPQPGEARL AALTAGDRVP WARCRQAYFG RGKNKQSLDA VEKAAFFVTL
DETEEGYRSE DPDTSMDSYA KSLLHGRCYD RWFDKSFTFV VFKNGKMGLN AEHSWADAPI
VAHLWEYVMS IDSLQLGYAE DGHCKGDINP NIPYPTRLQW DIPGECQEVI ETSLNTANLL
ANDVDFHSFP FVAFGKGIIK KCRTSPDAFV QLALQLAHYK DMGKFCLTYE ASMTRLFREG
RTETVRSCTT ESCDFVRAMV DPAQTVEQRL KLFKLASEKH QHMYRLAMTG SGIDRHLFCL
YVVSKYLAVE SPFLKEVLSE PWRLSTSQTP QQQVELFDLE NNPEYVSSGG GFGPVADDGY
GVSYILVGEN LINFHISSKF SCPETGIISQ GPSSDT*
mutated AA sequence MAEAHQAVAF QFTVTPDGID LRLSHEALRQ IYLSGLHSWK KKFIRFKNGI ITGVYPASPS
SWLIVVVGVM TTMYAKIDPS LGIIAKINRT LETANCMSSQ TKNVVSGVLF GTGLWVALIV
TMRYSLKVLL SYHGWMFTEH GKMSRATKIW MGMVKIFSGR KPMLYSFQTS LPRLPVPAVK
DTVNRYLQSV RPLMKEEDFK RMTALAQDFA VGLGPRLQWY LKLKSWWATN YVSDWWEEYI
YLRGRGPLMV NSNYYAMDLL YILPTHIQAA RAGNAIHAIL LYRRKLDREE IKPIRLLGST
IPLCSAQWER MFNTSRIPGE ETDTIQHMRD SKHIVVYHRG RYFKVWLYHD GRLLKPREME
QQMQRILDNT SEPQPGEARL AALTAGDRVP WARCRQAYFG RGKNKQSLDA VEKAAFFVTL
DETEEGYRSE DPDTSMDSYA KSLLHGRCYD RWFDKSFTFV VFKNGKMGLN AEHSWADALI
VAHLWEYVMS IDSLQLGYAE DGHCKGDINP NIPYPTRLQW DIPGECQEVI ETSLNTANLL
ANDVDFHSFP FVAFGKGIIK KCRTSPDAFV QLALQLAHYK DMGKFCLTYE ASMTRLFREG
RTETVRSCTT ESCDFVRAMV DPAQTVEQRL KLFKLASEKH QHMYRLAMTG SGIDRHLFCL
YVVSKYLAVE SPFLKEVLSE PWRLSTSQTP QQQVELFDLE NNPEYVSSGG GFGPVADDGY
GVSYILVGEN LINFHISSKF SCPETGIISQ GPSSDT*
speed 1.37 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: 0.999999999996992 (classification due to ClinVar, real probability is shown anyway)      (explain)
Summary
  • amino acid sequence changed
  • known disease mutation at this position (HGMD CM016082)
  • known disease mutation: rs65644 (pathogenic)
  • protein features (might be) affected
hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr11:68548130G>AN/A show variant in all transcripts   IGV
HGNC symbol CPT1A
Ensembl transcript ID ENST00000539743
Genbank transcript ID N/A
UniProt peptide P50416
alteration type single base exchange
alteration region CDS
DNA changes c.1436C>T
cDNA.1465C>T
g.63749C>T
AA changes P479L Score: 98 explain score(s)
position(s) of altered AA
if AA alteration in CDS
479
frameshift no
known variant Reference ID: rs80356779
databasehomozygous (A/A)heterozygousallele carriers
1000G---
ExAC022

known disease mutation: rs65644 (pathogenic for CARNITINE PALMITOYLTRANSFERASE IA POLYMORPHISM|CPT1A ARCTIC VARIANT|Carnitine palmitoyltransferase type I deficiency|Carnitine palmitoyltransferase 1A deficiency|not provided) dbSNP  NCBI variation viewer
known disease mutation at this position, please check HGMD for details (HGMD ID CM016082)

known disease mutation at this position, please check HGMD for details (HGMD ID CM016082)
known disease mutation at this position, please check HGMD for details (HGMD ID CM016082)
regulatory features H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
H3K4me1, Histone, Histone 3 Lysine 4 Mono-Methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)-0.6690.75
6.0731
(flanking)6.0731
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 23
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      479GLNAEHSWADAPIVAHLWEYVMSI
mutated  not conserved    479GLNAEHSWADALIVAHLWEYVMS
Ptroglodytes  all identical  ENSPTRG00000003987  479GLNAEHSWADAPIVAHLWEYVMS
Mmulatta  all identical  ENSMMUG00000001780  479GINAEHSWADAPIMAHLWEYVMS
Fcatus  no homologue    
Mmusculus  all identical  ENSMUSG00000024900  479GINAEHSWADAPIVGHLWEYVMA
Ggallus  all identical  ENSGALG00000007077  479GLNAEHSWADAPIVGHLWENVMA
Trubripes  all identical  ENSTRUG00000009681  482APIVGHLWEHVLS
Drerio  all identical  ENSDARG00000062054  479GLNAEHSWADAPIVGHLWEQVLS
Dmelanogaster  not conserved  FBgn0261862  477TWSDAAIASHMWENLIV
Celegans  not conserved  Y46G5A.17  480AVMAHFTEWSLL
Xtropicalis  no homologue    
protein features
start (aa)end (aa)featuredetails 
123773TOPO_DOMCytoplasmic (Potential).lost
479479CONFLICTP -> Q (in Ref. 1; AAC41748).lost
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 2322 / 2322
position (AA) of stopcodon in wt / mu AA sequence 774 / 774
position of stopcodon in wt / mu cDNA 2351 / 2351
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 30 / 30
chromosome 11
strand -1
last intron/exon boundary 2265
theoretical NMD boundary in CDS 2185
length of CDS 2322
coding sequence (CDS) position 1436
cDNA position
(for ins/del: last normal base / first normal base)
1465
gDNA position
(for ins/del: last normal base / first normal base)
63749
chromosomal position
(for ins/del: last normal base / first normal base)
68548130
original gDNA sequence snippet ACACTCCTGGGCAGATGCGCCGATCGTGGCCCACCTTTGGG
altered gDNA sequence snippet ACACTCCTGGGCAGATGCGCTGATCGTGGCCCACCTTTGGG
original cDNA sequence snippet ACACTCCTGGGCAGATGCGCCGATCGTGGCCCACCTTTGGG
altered cDNA sequence snippet ACACTCCTGGGCAGATGCGCTGATCGTGGCCCACCTTTGGG
wildtype AA sequence MAEAHQAVAF QFTVTPDGID LRLSHEALRQ IYLSGLHSWK KKFIRFKNGI ITGVYPASPS
SWLIVVVGVM TTMYAKIDPS LGIIAKINRT LETANCMSSQ TKNVVSGVLF GTGLWVALIV
TMRYSLKVLL SYHGWMFTEH GKMSRATKIW MGMVKIFSGR KPMLYSFQTS LPRLPVPAVK
DTVNRYLQSV RPLMKEEDFK RMTALAQDFA VGLGPRLQWY LKLKSWWATN YVSDWWEEYI
YLRGRGPLMV NSNYYAMDLL YILPTHIQAA RAGNAIHAIL LYRRKLDREE IKPIRLLGST
IPLCSAQWER MFNTSRIPGE ETDTIQHMRD SKHIVVYHRG RYFKVWLYHD GRLLKPREME
QQMQRILDNT SEPQPGEARL AALTAGDRVP WARCRQAYFG RGKNKQSLDA VEKAAFFVTL
DETEEGYRSE DPDTSMDSYA KSLLHGRCYD RWFDKSFTFV VFKNGKMGLN AEHSWADAPI
VAHLWEYVMS IDSLQLGYAE DGHCKGDINP NIPYPTRLQW DIPGECQEVI ETSLNTANLL
ANDVDFHSFP FVAFGKGIIK KCRTSPDAFV QLALQLAHYK DMGKFCLTYE ASMTRLFREG
RTETVRSCTT ESCDFVRAMV DPAQTVEQRL KLFKLASEKH QHMYRLAMTG SGIDRHLFCL
YVVSKYLAVE SPFLKEVLSE PWRLSTSQTP QQQVELFDLE NNPEYVSSGG GFGPVADDGY
GVSYILVGEN LINFHISSKF SCPETDSHRF GRHLKEAMTD IITLFGLSSN SKK*
mutated AA sequence MAEAHQAVAF QFTVTPDGID LRLSHEALRQ IYLSGLHSWK KKFIRFKNGI ITGVYPASPS
SWLIVVVGVM TTMYAKIDPS LGIIAKINRT LETANCMSSQ TKNVVSGVLF GTGLWVALIV
TMRYSLKVLL SYHGWMFTEH GKMSRATKIW MGMVKIFSGR KPMLYSFQTS LPRLPVPAVK
DTVNRYLQSV RPLMKEEDFK RMTALAQDFA VGLGPRLQWY LKLKSWWATN YVSDWWEEYI
YLRGRGPLMV NSNYYAMDLL YILPTHIQAA RAGNAIHAIL LYRRKLDREE IKPIRLLGST
IPLCSAQWER MFNTSRIPGE ETDTIQHMRD SKHIVVYHRG RYFKVWLYHD GRLLKPREME
QQMQRILDNT SEPQPGEARL AALTAGDRVP WARCRQAYFG RGKNKQSLDA VEKAAFFVTL
DETEEGYRSE DPDTSMDSYA KSLLHGRCYD RWFDKSFTFV VFKNGKMGLN AEHSWADALI
VAHLWEYVMS IDSLQLGYAE DGHCKGDINP NIPYPTRLQW DIPGECQEVI ETSLNTANLL
ANDVDFHSFP FVAFGKGIIK KCRTSPDAFV QLALQLAHYK DMGKFCLTYE ASMTRLFREG
RTETVRSCTT ESCDFVRAMV DPAQTVEQRL KLFKLASEKH QHMYRLAMTG SGIDRHLFCL
YVVSKYLAVE SPFLKEVLSE PWRLSTSQTP QQQVELFDLE NNPEYVSSGG GFGPVADDGY
GVSYILVGEN LINFHISSKF SCPETDSHRF GRHLKEAMTD IITLFGLSSN SKK*
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: 0.999999999996992 (classification due to ClinVar, real probability is shown anyway)      (explain)
Summary
  • amino acid sequence changed
  • known disease mutation at this position (HGMD CM016082)
  • known disease mutation: rs65644 (pathogenic)
  • protein features (might be) affected
hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr11:68548130G>AN/A show variant in all transcripts   IGV
HGNC symbol CPT1A
Ensembl transcript ID ENST00000376618
Genbank transcript ID NM_001031847
UniProt peptide P50416
alteration type single base exchange
alteration region CDS
DNA changes c.1436C>T
cDNA.1606C>T
g.63749C>T
AA changes P479L Score: 98 explain score(s)
position(s) of altered AA
if AA alteration in CDS
479
frameshift no
known variant Reference ID: rs80356779
databasehomozygous (A/A)heterozygousallele carriers
1000G---
ExAC022

known disease mutation: rs65644 (pathogenic for CARNITINE PALMITOYLTRANSFERASE IA POLYMORPHISM|CPT1A ARCTIC VARIANT|Carnitine palmitoyltransferase type I deficiency|Carnitine palmitoyltransferase 1A deficiency|not provided) dbSNP  NCBI variation viewer
known disease mutation at this position, please check HGMD for details (HGMD ID CM016082)

known disease mutation at this position, please check HGMD for details (HGMD ID CM016082)
known disease mutation at this position, please check HGMD for details (HGMD ID CM016082)
regulatory features H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
H3K4me1, Histone, Histone 3 Lysine 4 Mono-Methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)-0.6690.75
6.0731
(flanking)6.0731
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 23
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      479GLNAEHSWADAPIVAHLWEYVMSI
mutated  not conserved    479GLNAEHSWADALIVAHLWEYVMS
Ptroglodytes  all identical  ENSPTRG00000003987  479GLNAEHSWADAPIVAHLWEYVMS
Mmulatta  all identical  ENSMMUG00000001780  479GINAEHSWADAPIMAHLWEYVMS
Fcatus  no homologue    
Mmusculus  all identical  ENSMUSG00000024900  479GINAEHSWADAPIVGHLWEYVMA
Ggallus  all identical  ENSGALG00000007077  479GLNAEHSWADAPIVGHLWENVMA
Trubripes  all identical  ENSTRUG00000009681  482APIVGHLWEHVLS
Drerio  all identical  ENSDARG00000062054  479GLNAEHSWADAPIVGHLWEQVLS
Dmelanogaster  not conserved  FBgn0261862  477TWSDAAIASHMWENLIV
Celegans  not conserved  Y46G5A.17  480AVMAHFTEWSLL
Xtropicalis  no homologue    
protein features
start (aa)end (aa)featuredetails 
123773TOPO_DOMCytoplasmic (Potential).lost
479479CONFLICTP -> Q (in Ref. 1; AAC41748).lost
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 2271 / 2271
position (AA) of stopcodon in wt / mu AA sequence 757 / 757
position of stopcodon in wt / mu cDNA 2441 / 2441
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 171 / 171
chromosome 11
strand -1
last intron/exon boundary 2406
theoretical NMD boundary in CDS 2185
length of CDS 2271
coding sequence (CDS) position 1436
cDNA position
(for ins/del: last normal base / first normal base)
1606
gDNA position
(for ins/del: last normal base / first normal base)
63749
chromosomal position
(for ins/del: last normal base / first normal base)
68548130
original gDNA sequence snippet ACACTCCTGGGCAGATGCGCCGATCGTGGCCCACCTTTGGG
altered gDNA sequence snippet ACACTCCTGGGCAGATGCGCTGATCGTGGCCCACCTTTGGG
original cDNA sequence snippet ACACTCCTGGGCAGATGCGCCGATCGTGGCCCACCTTTGGG
altered cDNA sequence snippet ACACTCCTGGGCAGATGCGCTGATCGTGGCCCACCTTTGGG
wildtype AA sequence MAEAHQAVAF QFTVTPDGID LRLSHEALRQ IYLSGLHSWK KKFIRFKNGI ITGVYPASPS
SWLIVVVGVM TTMYAKIDPS LGIIAKINRT LETANCMSSQ TKNVVSGVLF GTGLWVALIV
TMRYSLKVLL SYHGWMFTEH GKMSRATKIW MGMVKIFSGR KPMLYSFQTS LPRLPVPAVK
DTVNRYLQSV RPLMKEEDFK RMTALAQDFA VGLGPRLQWY LKLKSWWATN YVSDWWEEYI
YLRGRGPLMV NSNYYAMDLL YILPTHIQAA RAGNAIHAIL LYRRKLDREE IKPIRLLGST
IPLCSAQWER MFNTSRIPGE ETDTIQHMRD SKHIVVYHRG RYFKVWLYHD GRLLKPREME
QQMQRILDNT SEPQPGEARL AALTAGDRVP WARCRQAYFG RGKNKQSLDA VEKAAFFVTL
DETEEGYRSE DPDTSMDSYA KSLLHGRCYD RWFDKSFTFV VFKNGKMGLN AEHSWADAPI
VAHLWEYVMS IDSLQLGYAE DGHCKGDINP NIPYPTRLQW DIPGECQEVI ETSLNTANLL
ANDVDFHSFP FVAFGKGIIK KCRTSPDAFV QLALQLAHYK DMGKFCLTYE ASMTRLFREG
RTETVRSCTT ESCDFVRAMV DPAQTVEQRL KLFKLASEKH QHMYRLAMTG SGIDRHLFCL
YVVSKYLAVE SPFLKEVLSE PWRLSTSQTP QQQVELFDLE NNPEYVSSGG GFGPVADDGY
GVSYILVGEN LINFHISSKF SCPETGIISQ GPSSDT*
mutated AA sequence MAEAHQAVAF QFTVTPDGID LRLSHEALRQ IYLSGLHSWK KKFIRFKNGI ITGVYPASPS
SWLIVVVGVM TTMYAKIDPS LGIIAKINRT LETANCMSSQ TKNVVSGVLF GTGLWVALIV
TMRYSLKVLL SYHGWMFTEH GKMSRATKIW MGMVKIFSGR KPMLYSFQTS LPRLPVPAVK
DTVNRYLQSV RPLMKEEDFK RMTALAQDFA VGLGPRLQWY LKLKSWWATN YVSDWWEEYI
YLRGRGPLMV NSNYYAMDLL YILPTHIQAA RAGNAIHAIL LYRRKLDREE IKPIRLLGST
IPLCSAQWER MFNTSRIPGE ETDTIQHMRD SKHIVVYHRG RYFKVWLYHD GRLLKPREME
QQMQRILDNT SEPQPGEARL AALTAGDRVP WARCRQAYFG RGKNKQSLDA VEKAAFFVTL
DETEEGYRSE DPDTSMDSYA KSLLHGRCYD RWFDKSFTFV VFKNGKMGLN AEHSWADALI
VAHLWEYVMS IDSLQLGYAE DGHCKGDINP NIPYPTRLQW DIPGECQEVI ETSLNTANLL
ANDVDFHSFP FVAFGKGIIK KCRTSPDAFV QLALQLAHYK DMGKFCLTYE ASMTRLFREG
RTETVRSCTT ESCDFVRAMV DPAQTVEQRL KLFKLASEKH QHMYRLAMTG SGIDRHLFCL
YVVSKYLAVE SPFLKEVLSE PWRLSTSQTP QQQVELFDLE NNPEYVSSGG GFGPVADDGY
GVSYILVGEN LINFHISSKF SCPETGIISQ GPSSDT*
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
Yum, tasty mutations...

mutation t@sting

documentation

Prediction

disease causing

Model: simple_aae, prob: 0.999999999996992 (classification due to ClinVar, real probability is shown anyway)      (explain)
Summary
  • amino acid sequence changed
  • known disease mutation at this position (HGMD CM016082)
  • known disease mutation: rs65644 (pathogenic)
  • protein features (might be) affected
hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr11:68548130G>AN/A show variant in all transcripts   IGV
HGNC symbol CPT1A
Ensembl transcript ID ENST00000265641
Genbank transcript ID NM_001876
UniProt peptide P50416
alteration type single base exchange
alteration region CDS
DNA changes c.1436C>T
cDNA.1606C>T
g.63749C>T
AA changes P479L Score: 98 explain score(s)
position(s) of altered AA
if AA alteration in CDS
479
frameshift no
known variant Reference ID: rs80356779
databasehomozygous (A/A)heterozygousallele carriers
1000G---
ExAC022

known disease mutation: rs65644 (pathogenic for CARNITINE PALMITOYLTRANSFERASE IA POLYMORPHISM|CPT1A ARCTIC VARIANT|Carnitine palmitoyltransferase type I deficiency|Carnitine palmitoyltransferase 1A deficiency|not provided) dbSNP  NCBI variation viewer
known disease mutation at this position, please check HGMD for details (HGMD ID CM016082)

known disease mutation at this position, please check HGMD for details (HGMD ID CM016082)
known disease mutation at this position, please check HGMD for details (HGMD ID CM016082)
regulatory features H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
H3K4me1, Histone, Histone 3 Lysine 4 Mono-Methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)-0.6690.75
6.0731
(flanking)6.0731
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 23
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      479GLNAEHSWADAPIVAHLWEYVMSI
mutated  not conserved    479GLNAEHSWADALIVAHLWEYVMS
Ptroglodytes  all identical  ENSPTRG00000003987  479GLNAEHSWADAPIVAHLWEYVMS
Mmulatta  all identical  ENSMMUG00000001780  479GINAEHSWADAPIMAHLWEYVMS
Fcatus  no homologue    
Mmusculus  all identical  ENSMUSG00000024900  479GINAEHSWADAPIVGHLWEYVMA
Ggallus  all identical  ENSGALG00000007077  479GLNAEHSWADAPIVGHLWENVMA
Trubripes  all identical  ENSTRUG00000009681  482APIVGHLWEHVLS
Drerio  all identical  ENSDARG00000062054  479GLNAEHSWADAPIVGHLWEQVLS
Dmelanogaster  not conserved  FBgn0261862  477TWSDAAIASHMWENLIV
Celegans  not conserved  Y46G5A.17  480AVMAHFTEWSLL
Xtropicalis  no homologue    
protein features
start (aa)end (aa)featuredetails 
123773TOPO_DOMCytoplasmic (Potential).lost
479479CONFLICTP -> Q (in Ref. 1; AAC41748).lost
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 2322 / 2322
position (AA) of stopcodon in wt / mu AA sequence 774 / 774
position of stopcodon in wt / mu cDNA 2492 / 2492
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 171 / 171
chromosome 11
strand -1
last intron/exon boundary 2406
theoretical NMD boundary in CDS 2185
length of CDS 2322
coding sequence (CDS) position 1436
cDNA position
(for ins/del: last normal base / first normal base)
1606
gDNA position
(for ins/del: last normal base / first normal base)
63749
chromosomal position
(for ins/del: last normal base / first normal base)
68548130
original gDNA sequence snippet ACACTCCTGGGCAGATGCGCCGATCGTGGCCCACCTTTGGG
altered gDNA sequence snippet ACACTCCTGGGCAGATGCGCTGATCGTGGCCCACCTTTGGG
original cDNA sequence snippet ACACTCCTGGGCAGATGCGCCGATCGTGGCCCACCTTTGGG
altered cDNA sequence snippet ACACTCCTGGGCAGATGCGCTGATCGTGGCCCACCTTTGGG
wildtype AA sequence MAEAHQAVAF QFTVTPDGID LRLSHEALRQ IYLSGLHSWK KKFIRFKNGI ITGVYPASPS
SWLIVVVGVM TTMYAKIDPS LGIIAKINRT LETANCMSSQ TKNVVSGVLF GTGLWVALIV
TMRYSLKVLL SYHGWMFTEH GKMSRATKIW MGMVKIFSGR KPMLYSFQTS LPRLPVPAVK
DTVNRYLQSV RPLMKEEDFK RMTALAQDFA VGLGPRLQWY LKLKSWWATN YVSDWWEEYI
YLRGRGPLMV NSNYYAMDLL YILPTHIQAA RAGNAIHAIL LYRRKLDREE IKPIRLLGST
IPLCSAQWER MFNTSRIPGE ETDTIQHMRD SKHIVVYHRG RYFKVWLYHD GRLLKPREME
QQMQRILDNT SEPQPGEARL AALTAGDRVP WARCRQAYFG RGKNKQSLDA VEKAAFFVTL
DETEEGYRSE DPDTSMDSYA KSLLHGRCYD RWFDKSFTFV VFKNGKMGLN AEHSWADAPI
VAHLWEYVMS IDSLQLGYAE DGHCKGDINP NIPYPTRLQW DIPGECQEVI ETSLNTANLL
ANDVDFHSFP FVAFGKGIIK KCRTSPDAFV QLALQLAHYK DMGKFCLTYE ASMTRLFREG
RTETVRSCTT ESCDFVRAMV DPAQTVEQRL KLFKLASEKH QHMYRLAMTG SGIDRHLFCL
YVVSKYLAVE SPFLKEVLSE PWRLSTSQTP QQQVELFDLE NNPEYVSSGG GFGPVADDGY
GVSYILVGEN LINFHISSKF SCPETDSHRF GRHLKEAMTD IITLFGLSSN SKK*
mutated AA sequence MAEAHQAVAF QFTVTPDGID LRLSHEALRQ IYLSGLHSWK KKFIRFKNGI ITGVYPASPS
SWLIVVVGVM TTMYAKIDPS LGIIAKINRT LETANCMSSQ TKNVVSGVLF GTGLWVALIV
TMRYSLKVLL SYHGWMFTEH GKMSRATKIW MGMVKIFSGR KPMLYSFQTS LPRLPVPAVK
DTVNRYLQSV RPLMKEEDFK RMTALAQDFA VGLGPRLQWY LKLKSWWATN YVSDWWEEYI
YLRGRGPLMV NSNYYAMDLL YILPTHIQAA RAGNAIHAIL LYRRKLDREE IKPIRLLGST
IPLCSAQWER MFNTSRIPGE ETDTIQHMRD SKHIVVYHRG RYFKVWLYHD GRLLKPREME
QQMQRILDNT SEPQPGEARL AALTAGDRVP WARCRQAYFG RGKNKQSLDA VEKAAFFVTL
DETEEGYRSE DPDTSMDSYA KSLLHGRCYD RWFDKSFTFV VFKNGKMGLN AEHSWADALI
VAHLWEYVMS IDSLQLGYAE DGHCKGDINP NIPYPTRLQW DIPGECQEVI ETSLNTANLL
ANDVDFHSFP FVAFGKGIIK KCRTSPDAFV QLALQLAHYK DMGKFCLTYE ASMTRLFREG
RTETVRSCTT ESCDFVRAMV DPAQTVEQRL KLFKLASEKH QHMYRLAMTG SGIDRHLFCL
YVVSKYLAVE SPFLKEVLSE PWRLSTSQTP QQQVELFDLE NNPEYVSSGG GFGPVADDGY
GVSYILVGEN LINFHISSKF SCPETDSHRF GRHLKEAMTD IITLFGLSSN SKK*
speed 0.54 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