Yum, tasty mutations...

MutationTaster - study a chromosomal position

MTQE documentation
NEVER press reload or F5 - unless you want to start from the very beginning.
input seems to be ok - now mapping the variant to the different transcripts...
found 2 transcript(s)...
Querying Taster for transcript #1: ENST00000264381
Querying Taster for transcript #2: ENST00000540653
MT speed 1.94 s - this script 3.971081 s

Results


genesymbolpredictionprobabilitymodelprediction
problem
splicingClinVaramino acid changesvariant typedbSNP IDprotein lengthfile
BCHEdisease_causing_automatic0.999999999697187simple_aaeaffected0Y156Csingle base exchangers121918558show file
BCHEdisease_causing_automatic1without_aaeaffected0single base exchangers121918558show file

Taster files

Yum, tasty mutations...

mutation t@sting

documentation

Prediction

disease causing

Model: simple_aae, prob: 0.999999999697187 (classification due to ClinVar, real probability is shown anyway)      (explain)
Summary
  • amino acid sequence changed
  • known disease mutation at this position (HGMD CM970162)
  • known disease mutation: rs13227 (pathogenic)
  • protein features (might be) affected
  • splice site changes
hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr3:165548355T>CN/A show variant in all transcripts   IGV
HGNC symbol BCHE
Ensembl transcript ID ENST00000264381
Genbank transcript ID NM_000055
UniProt peptide P06276
alteration type single base exchange
alteration region CDS
DNA changes c.467A>G
cDNA.634A>G
g.6906A>G
AA changes Y156C Score: 194 explain score(s)
position(s) of altered AA
if AA alteration in CDS
156
frameshift no
known variant Reference ID: rs121918558
Allele 'C' was neither found in ExAC nor 1000G.
known disease mutation: rs13227 (pathogenic for Deficiency of butyrylcholine esterase) dbSNP  NCBI variation viewer
known disease mutation at this position, please check HGMD for details (HGMD ID CM970162)

known disease mutation at this position, please check HGMD for details (HGMD ID CM970162)
known disease mutation at this position, please check HGMD for details (HGMD ID CM970162)
regulatory features N/A
phyloP / phastCons
PhyloPPhastCons
(flanking)0.1410.997
4.6411
(flanking)4.6411
explain score(s) and/or inspect your position(s) in in UCSC Genome Browser
splice sites
effectgDNA positionscorewt detection sequence exon-intron border
Acc increased6915wt: 0.30 / mu: 0.38wt: TTTACATGTTTATGATGGCAAGTTTCTGGCTCGGGTTGAAA
mu: TTTACATGTTTGTGATGGCAAGTTTCTGGCTCGGGTTGAAA
 gcaa|GTTT
Acc increased6905wt: 0.44 / mu: 0.75wt: GAACATCATCTTTACATGTTTATGATGGCAAGTTTCTGGCT
mu: GAACATCATCTTTACATGTTTGTGATGGCAAGTTTCTGGCT
 gttt|ATGA
Acc marginally increased6903wt: 0.3791 / mu: 0.4011 (marginal change - not scored)wt: TGGAACATCATCTTTACATGTTTATGATGGCAAGTTTCTGG
mu: TGGAACATCATCTTTACATGTTTGTGATGGCAAGTTTCTGG
 atgt|TTAT
Donor gained69050.81mu: ATGTTTGTGATGGCA GTTT|gtga
distance from splice site 475
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      156GFQTGTSSLHVYDGKFLARVERVI
mutated  not conserved    156GFQTGTSSLHVCDGKFLARVERV
Ptroglodytes  all identical  ENSPTRG00000015593  156GFQTGTSSLHVYDGKFLARVERV
Mmulatta  all identical  ENSMMUG00000003742  156GFQTGTSSLHVYDGKFLARVERV
Fcatus  no homologue    
Mmusculus  all identical  ENSMUSG00000027792  157GFQTGTSSLPVYDGKFLARVERV
Ggallus  all identical  ENSGALG00000009478  156SFETGSTSLPVYDGKFLARVERV
Trubripes  all identical  ENSTRUG00000005322  152GFTTGTSSLELYDGRYLTKSEDV
Drerio  no homologue    
Dmelanogaster  all identical  FBgn0000024  186GFMTGSATLDIYNADIMAAVGNV
Celegans  all identical  W09B12.1  145GFWSGTATLDVYDGRILTV
Xtropicalis  all identical  ENSXETG00000006497  158SFETGTSSLDLYDGKFLARTERV
protein features
start (aa)end (aa)featuredetails 
154156HELIXlost
159165HELIXmight get lost (downstream of altered splice site)
168172STRANDmight get lost (downstream of altered splice site)
177181HELIXmight get lost (downstream of altered splice site)
190192STRANDmight get lost (downstream of altered splice site)
194209HELIXmight get lost (downstream of altered splice site)
210213HELIXmight get lost (downstream of altered splice site)
215225STRANDmight get lost (downstream of altered splice site)
226226ACT_SITEAcyl-ester intermediate.might get lost (downstream of altered splice site)
227237HELIXmight get lost (downstream of altered splice site)
239244HELIXmight get lost (downstream of altered splice site)
246252STRANDmight get lost (downstream of altered splice site)
258260TURNmight get lost (downstream of altered splice site)
264277HELIXmight get lost (downstream of altered splice site)
269269CARBOHYDN-linked (GlcNAc...).might get lost (downstream of altered splice site)
280280DISULFIDmight get lost (downstream of altered splice site)
284284CARBOHYDN-linked (GlcNAc...).might get lost (downstream of altered splice site)
285292HELIXmight get lost (downstream of altered splice site)
291291DISULFIDmight get lost (downstream of altered splice site)
297304HELIXmight get lost (downstream of altered splice site)
305307HELIXmight get lost (downstream of altered splice site)
308310STRANDmight get lost (downstream of altered splice site)
324326STRANDmight get lost (downstream of altered splice site)
331336HELIXmight get lost (downstream of altered splice site)
345350STRANDmight get lost (downstream of altered splice site)
352354STRANDmight get lost (downstream of altered splice site)
353353ACT_SITECharge relay system.might get lost (downstream of altered splice site)
355358HELIXmight get lost (downstream of altered splice site)
359361TURNmight get lost (downstream of altered splice site)
367369STRANDmight get lost (downstream of altered splice site)
369369CARBOHYDN-linked (GlcNAc...).might get lost (downstream of altered splice site)
375385HELIXmight get lost (downstream of altered splice site)
387389STRANDmight get lost (downstream of altered splice site)
391401HELIXmight get lost (downstream of altered splice site)
405408TURNmight get lost (downstream of altered splice site)
412425HELIXmight get lost (downstream of altered splice site)
427438HELIXmight get lost (downstream of altered splice site)
428428DISULFIDmight get lost (downstream of altered splice site)
439441TURNmight get lost (downstream of altered splice site)
444449STRANDmight get lost (downstream of altered splice site)
460462HELIXmight get lost (downstream of altered splice site)
466466ACT_SITECharge relay system.might get lost (downstream of altered splice site)
466469TURNmight get lost (downstream of altered splice site)
470473HELIXmight get lost (downstream of altered splice site)
476478HELIXmight get lost (downstream of altered splice site)
480482HELIXmight get lost (downstream of altered splice site)
483483CARBOHYDN-linked (GlcNAc...).might get lost (downstream of altered splice site)
486505HELIXmight get lost (downstream of altered splice site)
509509CARBOHYDN-linked (GlcNAc...).might get lost (downstream of altered splice site)
511514TURNmight get lost (downstream of altered splice site)
513513CARBOHYDN-linked (GlcNAc...).might get lost (downstream of altered splice site)
514514CARBOHYDN-linked (GlcNAc...).might get lost (downstream of altered splice site)
523525TURNmight get lost (downstream of altered splice site)
527531STRANDmight get lost (downstream of altered splice site)
538541STRANDmight get lost (downstream of altered splice site)
544551HELIXmight get lost (downstream of altered splice site)
547547DISULFIDmight get lost (downstream of altered splice site)
552555TURNmight get lost (downstream of altered splice site)
599599DISULFIDInterchain.might get lost (downstream of altered splice site)
599599DISULFIDInterchain.might get lost (downstream of altered splice site)
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 1809 / 1809
position (AA) of stopcodon in wt / mu AA sequence 603 / 603
position of stopcodon in wt / mu cDNA 1976 / 1976
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 168 / 168
chromosome 3
strand -1
last intron/exon boundary 1852
theoretical NMD boundary in CDS 1634
length of CDS 1809
coding sequence (CDS) position 467
cDNA position
(for ins/del: last normal base / first normal base)
634
gDNA position
(for ins/del: last normal base / first normal base)
6906
chromosomal position
(for ins/del: last normal base / first normal base)
165548355
original gDNA sequence snippet AACATCATCTTTACATGTTTATGATGGCAAGTTTCTGGCTC
altered gDNA sequence snippet AACATCATCTTTACATGTTTGTGATGGCAAGTTTCTGGCTC
original cDNA sequence snippet AACATCATCTTTACATGTTTATGATGGCAAGTTTCTGGCTC
altered cDNA sequence snippet AACATCATCTTTACATGTTTGTGATGGCAAGTTTCTGGCTC
wildtype AA sequence MHSKVTIICI RFLFWFLLLC MLIGKSHTED DIIIATKNGK VRGMNLTVFG GTVTAFLGIP
YAQPPLGRLR FKKPQSLTKW SDIWNATKYA NSCCQNIDQS FPGFHGSEMW NPNTDLSEDC
LYLNVWIPAP KPKNATVLIW IYGGGFQTGT SSLHVYDGKF LARVERVIVV SMNYRVGALG
FLALPGNPEA PGNMGLFDQQ LALQWVQKNI AAFGGNPKSV TLFGESAGAA SVSLHLLSPG
SHSLFTRAIL QSGSFNAPWA VTSLYEARNR TLNLAKLTGC SRENETEIIK CLRNKDPQEI
LLNEAFVVPY GTPLSVNFGP TVDGDFLTDM PDILLELGQF KKTQILVGVN KDEGTAFLVY
GAPGFSKDNN SIITRKEFQE GLKIFFPGVS EFGKESILFH YTDWVDDQRP ENYREALGDV
VGDYNFICPA LEFTKKFSEW GNNAFFYYFE HRSSKLPWPE WMGVMHGYEI EFVFGLPLER
RDNYTKAEEI LSRSIVKRWA NFAKYGNPNE TQNNSTSWPV FKSTEQKYLT LNTESTRIMT
KLRAQQCRFW TSFFPKVLEM TGNIDEAEWE WKAGFHRWNN YMMDWKNQFN DYTSKKESCV
GL*
mutated AA sequence MHSKVTIICI RFLFWFLLLC MLIGKSHTED DIIIATKNGK VRGMNLTVFG GTVTAFLGIP
YAQPPLGRLR FKKPQSLTKW SDIWNATKYA NSCCQNIDQS FPGFHGSEMW NPNTDLSEDC
LYLNVWIPAP KPKNATVLIW IYGGGFQTGT SSLHVCDGKF LARVERVIVV SMNYRVGALG
FLALPGNPEA PGNMGLFDQQ LALQWVQKNI AAFGGNPKSV TLFGESAGAA SVSLHLLSPG
SHSLFTRAIL QSGSFNAPWA VTSLYEARNR TLNLAKLTGC SRENETEIIK CLRNKDPQEI
LLNEAFVVPY GTPLSVNFGP TVDGDFLTDM PDILLELGQF KKTQILVGVN KDEGTAFLVY
GAPGFSKDNN SIITRKEFQE GLKIFFPGVS EFGKESILFH YTDWVDDQRP ENYREALGDV
VGDYNFICPA LEFTKKFSEW GNNAFFYYFE HRSSKLPWPE WMGVMHGYEI EFVFGLPLER
RDNYTKAEEI LSRSIVKRWA NFAKYGNPNE TQNNSTSWPV FKSTEQKYLT LNTESTRIMT
KLRAQQCRFW TSFFPKVLEM TGNIDEAEWE WKAGFHRWNN YMMDWKNQFN DYTSKKESCV
GL*
speed 1.06 s
All positions are in basepairs (bp) if not explicitly stated differently.
AA/aa: amino acid; CDS: coding sequence; mu: mutated; NMD: nonsense-mediated mRNA decay; nt: nucleotide; wt: wildtype; TGP: 1000 Genomes Project
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Yum, tasty mutations...

mutation t@sting

documentation

Prediction

disease causing

Model: without_aae, prob: 1 (classification due to ClinVar, real probability is shown anyway)      (explain)
Summary
  • known disease mutation at this position (HGMD CM970162)
  • known disease mutation: rs13227 (pathogenic)
  • protein features (might be) affected
  • splice site changes
hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr3:165548355T>CN/A show variant in all transcripts   IGV
HGNC symbol BCHE
Ensembl transcript ID ENST00000540653
Genbank transcript ID N/A
UniProt peptide P06276
alteration type single base exchange
alteration region intron
DNA changes g.6906A>G
AA changes N/A
position(s) of altered AA
if AA alteration in CDS
N/A
frameshift N/A
known variant Reference ID: rs121918558
Allele 'C' was neither found in ExAC nor 1000G.
known disease mutation: rs13227 (pathogenic for Deficiency of butyrylcholine esterase) dbSNP  NCBI variation viewer
known disease mutation at this position, please check HGMD for details (HGMD ID CM970162)

known disease mutation at this position, please check HGMD for details (HGMD ID CM970162)
known disease mutation at this position, please check HGMD for details (HGMD ID CM970162)
regulatory features N/A
phyloP / phastCons
PhyloPPhastCons
(flanking)0.1410.997
4.6411
(flanking)4.6411
explain score(s) and/or inspect your position(s) in in UCSC Genome Browser
splice sites splice site change before start ATG (at aa -31) |
effectgDNA positionscoredetection sequence  exon-intron border
Acc increased6915wt: 0.30 / mu: 0.38wt: TTTACATGTTTATGATGGCAAGTTTCTGGCTCGGGTTGAAA
mu: TTTACATGTTTGTGATGGCAAGTTTCTGGCTCGGGTTGAAA
 gcaa|GTTT
Acc increased6905wt: 0.44 / mu: 0.75wt: GAACATCATCTTTACATGTTTATGATGGCAAGTTTCTGGCT
mu: GAACATCATCTTTACATGTTTGTGATGGCAAGTTTCTGGCT
 gttt|ATGA
Acc marginally increased6903wt: 0.3791 / mu: 0.4011 (marginal change - not scored)wt: TGGAACATCATCTTTACATGTTTATGATGGCAAGTTTCTGG
mu: TGGAACATCATCTTTACATGTTTGTGATGGCAAGTTTCTGG
 atgt|TTAT
Donor gained69050.81mu: ATGTTTGTGATGGCA GTTT|gtga
distance from splice site 6747
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
N/A
protein features
start (aa)end (aa)featuredetails 
128SIGNALmight get lost (downstream of altered splice site)
3336STRANDmight get lost (downstream of altered splice site)
3942STRANDmight get lost (downstream of altered splice site)
4448STRANDmight get lost (downstream of altered splice site)
4545CARBOHYDN-linked (GlcNAc...).might get lost (downstream of altered splice site)
5160STRANDmight get lost (downstream of altered splice site)
6769HELIXmight get lost (downstream of altered splice site)
8285STRANDmight get lost (downstream of altered splice site)
8585CARBOHYDN-linked (GlcNAc...).might get lost (downstream of altered splice site)
9393DISULFIDmight get lost (downstream of altered splice site)
105108HELIXmight get lost (downstream of altered splice site)
116118STRANDmight get lost (downstream of altered splice site)
120120DISULFIDmight get lost (downstream of altered splice site)
122130STRANDmight get lost (downstream of altered splice site)
133141STRANDmight get lost (downstream of altered splice site)
134134CARBOHYDN-linked (GlcNAc...).might get lost (downstream of altered splice site)
144145REGIONSubstrate binding.might get lost (downstream of altered splice site)
145147TURNmight get lost (downstream of altered splice site)
154156HELIXmight get lost (downstream of altered splice site)
159165HELIXmight get lost (downstream of altered splice site)
168172STRANDmight get lost (downstream of altered splice site)
177181HELIXmight get lost (downstream of altered splice site)
190192STRANDmight get lost (downstream of altered splice site)
194209HELIXmight get lost (downstream of altered splice site)
210213HELIXmight get lost (downstream of altered splice site)
215225STRANDmight get lost (downstream of altered splice site)
226226ACT_SITEAcyl-ester intermediate.might get lost (downstream of altered splice site)
227237HELIXmight get lost (downstream of altered splice site)
239244HELIXmight get lost (downstream of altered splice site)
246252STRANDmight get lost (downstream of altered splice site)
258260TURNmight get lost (downstream of altered splice site)
264277HELIXmight get lost (downstream of altered splice site)
269269CARBOHYDN-linked (GlcNAc...).might get lost (downstream of altered splice site)
280280DISULFIDmight get lost (downstream of altered splice site)
284284CARBOHYDN-linked (GlcNAc...).might get lost (downstream of altered splice site)
285292HELIXmight get lost (downstream of altered splice site)
291291DISULFIDmight get lost (downstream of altered splice site)
297304HELIXmight get lost (downstream of altered splice site)
305307HELIXmight get lost (downstream of altered splice site)
308310STRANDmight get lost (downstream of altered splice site)
324326STRANDmight get lost (downstream of altered splice site)
331336HELIXmight get lost (downstream of altered splice site)
345350STRANDmight get lost (downstream of altered splice site)
352354STRANDmight get lost (downstream of altered splice site)
353353ACT_SITECharge relay system.might get lost (downstream of altered splice site)
355358HELIXmight get lost (downstream of altered splice site)
359361TURNmight get lost (downstream of altered splice site)
367369STRANDmight get lost (downstream of altered splice site)
369369CARBOHYDN-linked (GlcNAc...).might get lost (downstream of altered splice site)
375385HELIXmight get lost (downstream of altered splice site)
387389STRANDmight get lost (downstream of altered splice site)
391401HELIXmight get lost (downstream of altered splice site)
405408TURNmight get lost (downstream of altered splice site)
412425HELIXmight get lost (downstream of altered splice site)
427438HELIXmight get lost (downstream of altered splice site)
428428DISULFIDmight get lost (downstream of altered splice site)
439441TURNmight get lost (downstream of altered splice site)
444449STRANDmight get lost (downstream of altered splice site)
460462HELIXmight get lost (downstream of altered splice site)
466466ACT_SITECharge relay system.might get lost (downstream of altered splice site)
466469TURNmight get lost (downstream of altered splice site)
470473HELIXmight get lost (downstream of altered splice site)
476478HELIXmight get lost (downstream of altered splice site)
480482HELIXmight get lost (downstream of altered splice site)
483483CARBOHYDN-linked (GlcNAc...).might get lost (downstream of altered splice site)
486505HELIXmight get lost (downstream of altered splice site)
509509CARBOHYDN-linked (GlcNAc...).might get lost (downstream of altered splice site)
511514TURNmight get lost (downstream of altered splice site)
513513CARBOHYDN-linked (GlcNAc...).might get lost (downstream of altered splice site)
514514CARBOHYDN-linked (GlcNAc...).might get lost (downstream of altered splice site)
523525TURNmight get lost (downstream of altered splice site)
527531STRANDmight get lost (downstream of altered splice site)
538541STRANDmight get lost (downstream of altered splice site)
544551HELIXmight get lost (downstream of altered splice site)
547547DISULFIDmight get lost (downstream of altered splice site)
552555TURNmight get lost (downstream of altered splice site)
599599DISULFIDInterchain.might get lost (downstream of altered splice site)
599599DISULFIDInterchain.might get lost (downstream of altered splice site)
length of protein N/A
AA sequence altered N/A
position of stopcodon in wt / mu CDS N/A
position (AA) of stopcodon in wt / mu AA sequence N/A
position of stopcodon in wt / mu cDNA N/A
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 205 / 205
chromosome 3
strand -1
last intron/exon boundary 275
theoretical NMD boundary in CDS 20
length of CDS 195
coding sequence (CDS) position N/A
cDNA position
(for ins/del: last normal base / first normal base)
N/A
gDNA position
(for ins/del: last normal base / first normal base)
6906
chromosomal position
(for ins/del: last normal base / first normal base)
165548355
original gDNA sequence snippet AACATCATCTTTACATGTTTATGATGGCAAGTTTCTGGCTC
altered gDNA sequence snippet AACATCATCTTTACATGTTTGTGATGGCAAGTTTCTGGCTC
original cDNA sequence snippet N/A
altered cDNA sequence snippet N/A
wildtype AA sequence MTKLRAQQCR FWTSFFPKVL EMTGNIDEAE WEWKAGFHRW NNYMMDWKNQ FNDYTSKKES
CVGL*
mutated AA sequence N/A
speed 0.88 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