Yum, tasty mutations...

mutation t@sting

 documentation

Prediction

disease causing

 Model: simple_aae, prob: 0.999999999965333 (classification due to ClinVar, real probability is shown anyway)      (explain)
Summary
  • amino acid sequence changed
  • known disease mutation at this position (HGMD CM032577)
  • known disease mutation at this position (HGMD CM096860)
  • known disease mutation at this position (HGMD CM920305)
  • known disease mutation: rs16134 (pathogenic)
  • protein features (might be) affected
 hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr7:44187429G>AN/A show variant in all transcripts   IGV
HGNC symbol GCK
Ensembl transcript ID ENST00000437084
Genbank transcript ID N/A
UniProt peptide P35557
alteration type single base exchange
alteration region CDS
DNA changes c.632C>T
cDNA.666C>T
g.50341C>T
AA changes T211M Score: 81 explain score(s)
position(s) of altered AA
if AA alteration in CDS		 211
frameshift no
known variant Reference ID: rs80356655
databasehomozygous (A/A)heterozygousallele carriers
1000G---
ExAC011

known disease mutation: rs16134 (pathogenic for Maturity-onset diabetes of the young, type 2|Permanent neonatal diabetes mellitus 1|not provided) dbSNP  NCBI variation viewer
known disease mutation at this position, please check HGMD for details (HGMD ID CM920305)

known disease mutation at this position, please check HGMD for details (HGMD ID CM920305)
known disease mutation at this position, please check HGMD for details (HGMD ID CM032577)

known disease mutation at this position, please check HGMD for details (HGMD ID CM920305)
known disease mutation at this position, please check HGMD for details (HGMD ID CM032577)
known disease mutation at this position, please check HGMD for details (HGMD ID CM096860)

known disease mutation at this position, please check HGMD for details (HGMD ID CM920305)
known disease mutation at this position, please check HGMD for details (HGMD ID CM032577)
known disease mutation at this position, please check HGMD for details (HGMD ID CM096860)
known disease mutation at this position, please check HGMD for details (HGMD ID CM032577)

known disease mutation at this position, please check HGMD for details (HGMD ID CM920305)
known disease mutation at this position, please check HGMD for details (HGMD ID CM032577)
known disease mutation at this position, please check HGMD for details (HGMD ID CM096860)
known disease mutation at this position, please check HGMD for details (HGMD ID CM032577)
known disease mutation at this position, please check HGMD for details (HGMD ID CM096860)

known disease mutation at this position, please check HGMD for details (HGMD ID CM920305)
known disease mutation at this position, please check HGMD for details (HGMD ID CM032577)
known disease mutation at this position, please check HGMD for details (HGMD ID CM096860)
known disease mutation at this position, please check HGMD for details (HGMD ID CM032577)
known disease mutation at this position, please check HGMD for details (HGMD ID CM096860)
known disease mutation at this position, please check HGMD for details (HGMD ID CM920305)
regulatory features DNase1, Open Chromatin, DNase1 Hypersensitive Site
E2F6, Transcription Factor, E2F6 Transcription Factor Binding
H2AZ, Histone, Histone 2A variant Z
H3K27me3, Histone, Histone 3 Lysine 27 Tri-Methylation
Max, Transcription Factor, Max TF binding
PolII, Polymerase, RNA Polymerase II
Promoter Associated, Regulatory Feature, Promoter like regulatory feature
phyloP / phastCons
PhyloPPhastCons
(flanking)-3.5550.006
5.9151
(flanking)4.8821
explain score(s) and/or inspect your position(s) in in UCSC Genome Browser
splice sites
effectgDNA positionscorewt detection sequence exon-intron border
Acc marginally increased50337wt: 0.8603 / mu: 0.8819 (marginal change - not scored)wt: TCCCCCCGACCTCCACCCCAGGCACGGGCTGCAATGCCTGC
mu: TCCCCCCGACCTCCACCCCAGGCATGGGCTGCAATGCCTGC		 ccag|GCAC
Donor marginally increased50346wt: 0.8839 / mu: 0.9031 (marginal change - not scored)wt: CGGGCTGCAATGCCT
mu: TGGGCTGCAATGCCT		 GGCT|gcaa
distance from splice site 4
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      211DHQCEVGMIVGTGCNACYMEEMQN
mutated  not conserved    211DHQCEVGMIVGMGCNACYMEEMQ
Ptroglodytes  all identical  ENSPTRG00000019140  227DHQCEVGMIVGTGCNACYMEEMQ
Mmulatta  all identical  ENSMMUG00000002427  229DHQCEVGMIVGTGCNACYMEEMQ
Fcatus  all identical  ENSFCAG00000014361  213DRRCEVGMIVGTGCNACYMEEMH
Mmusculus  all identical  ENSMUSG00000041798  228DRQCEVGMIVGTGCNACYMEEMQ
Ggallus  no homologue    
Trubripes  no homologue    
Drerio  all identical  ENSDARG00000068006  238DRSCEVGMIVGTGCNACYMEEMR
Dmelanogaster  all identical  FBgn0001186  303NHNCKIGLIVGTGANACYMERVE
Celegans  all identical  F14B4.2  246ENSCQIGVIVGTGTNACYMERLD
Xtropicalis  all identical  ENSXETG00000019003  228DHHCEVGLIVGTGCNACYMEEMS
protein features
start (aa)end (aa)featuredetails 
205214HELIXlost
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 1347 / 1347
position (AA) of stopcodon in wt / mu AA sequence 449 / 449
position of stopcodon in wt / mu cDNA 1381 / 1381
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 35 / 35
chromosome 7
strand -1
last intron/exon boundary 1237
theoretical NMD boundary in CDS 1152
length of CDS 1347
coding sequence (CDS) position 632
cDNA position
(for ins/del: last normal base / first normal base)		 666
gDNA position
(for ins/del: last normal base / first normal base)		 50341
chromosomal position
(for ins/del: last normal base / first normal base)		 44187429
original gDNA sequence snippet CCCGACCTCCACCCCAGGCACGGGCTGCAATGCCTGCTACA
altered gDNA sequence snippet CCCGACCTCCACCCCAGGCATGGGCTGCAATGCCTGCTACA
original cDNA sequence snippet GGTCGGCATGATCGTGGGCACGGGCTGCAATGCCTGCTACA
altered cDNA sequence snippet GGTCGGCATGATCGTGGGCATGGGCTGCAATGCCTGCTACA
wildtype AA sequence MLDDRARMEA AKKEKVEQIL AEFQLQEEDL KKVMRRMQKE MDRGLRLETH EEASVKMLPT
YVRSTPEGSE VGDFLSLDLG GTNFRVMLVK VGEGEEGQWS VKTKHQMYSI PEDAMTGTAE
MMKHKKLPLG FTFSFPVRHE DIDKGILLNW TKGFKASGAE GNNVVGLLRD AIKRRGDFEM
DVVAMVNDTV ATMISCYYED HQCEVGMIVG TGCNACYMEE MQNVELVEGD EGRMCVNTEW
GAFGDSGELD EFLLEYDRLV DESSANPGQQ LYEKLIGGKY MGELVRLVLL RLVDENLLFH
GEASEQLRTR GAFETRFVSQ VESDTGDRKQ IYNILSTLGL RPSTTDCDIV RRACESVSTR
AAHMCSAGLA GVINRMRESR SEDVMRITVG VDGSVYKLHP SFKERFHASV RRLTPSCEIT
FIESEEGSGR GAALVSAVAC KKACMLGQ*
mutated AA sequence MLDDRARMEA AKKEKVEQIL AEFQLQEEDL KKVMRRMQKE MDRGLRLETH EEASVKMLPT
YVRSTPEGSE VGDFLSLDLG GTNFRVMLVK VGEGEEGQWS VKTKHQMYSI PEDAMTGTAE
MMKHKKLPLG FTFSFPVRHE DIDKGILLNW TKGFKASGAE GNNVVGLLRD AIKRRGDFEM
DVVAMVNDTV ATMISCYYED HQCEVGMIVG MGCNACYMEE MQNVELVEGD EGRMCVNTEW
GAFGDSGELD EFLLEYDRLV DESSANPGQQ LYEKLIGGKY MGELVRLVLL RLVDENLLFH
GEASEQLRTR GAFETRFVSQ VESDTGDRKQ IYNILSTLGL RPSTTDCDIV RRACESVSTR
AAHMCSAGLA GVINRMRESR SEDVMRITVG VDGSVYKLHP SFKERFHASV RRLTPSCEIT
FIESEEGSGR GAALVSAVAC KKACMLGQ*
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