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mutation t@sting

 documentation

Prediction

polymorphism

 Model: simple_aae, prob: 0.921989689952803      (explain)
Summary
  • amino acid sequence changed
  • known disease mutation at this position (HGMD CM081289)
  • protein features (might be) affected
  • splice site changes
 hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr2:233655527A>GN/A show variant in all transcripts   IGV
HGNC symbol GIGYF2
Ensembl transcript ID ENST00000373563
Genbank transcript ID N/A
UniProt peptide Q6Y7W6
alteration type single base exchange
alteration region CDS
DNA changes c.832A>G
cDNA.1027A>G
g.93519A>G
AA changes I278V Score: 29 explain score(s)
position(s) of altered AA
if AA alteration in CDS		 278
frameshift no
known variant Reference ID: rs118203904
databasehomozygous (G/G)heterozygousallele carriers
1000G011
ExAC02222

known disease mutation at this position, please check HGMD for details (HGMD ID CM081289)

known disease mutation at this position, please check HGMD for details (HGMD ID CM081289)
known disease mutation at this position, please check HGMD for details (HGMD ID CM081289)
regulatory features H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)3.2391
0.4921
(flanking)3.3351
explain score(s) and/or inspect your position(s) in in UCSC Genome Browser
splice sites
effectgDNA positionscorewt detection sequence exon-intron border
Donor marginally increased93516wt: 0.7236 / mu: 0.7424 (marginal change - not scored)wt: GTGGGAGCATAGATG
mu: GTGGGAGCGTAGATG		 GGGA|gcat
Donor gained935130.66mu: GCAGTGGGAGCGTAG AGTG|ggag
distance from splice site 99
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      278GYRRVRSGSGSIDDDRDSLPEWCL
mutated  all conserved    278GYRRVRSGSGSVDDDRDSLPEWC
Ptroglodytes  all identical  ENSPTRG00000028976  300GYRRVRSGSGSIDDDRDSLPEWC
Mmulatta  all identical  ENSMMUG00000012211  312GSIDDDRDSLPEWC
Fcatus  no homologue    
Mmusculus  all identical  ENSMUSG00000048000  279GYRRVRSGSGSIDDDRDSLPEWC
Ggallus  not conserved  ENSGALG00000001482  467KRREEEELA------RRKQEEAL
Trubripes  all conserved  ENSTRUG00000008935  293GYRRPRSGSGSLEDER
Drerio  not conserved  ENSDARG00000009735  285GYRRPRSGSGSAEEERDSLPE
Dmelanogaster  all identical  FBgn0039936  319GIGAAE-GVGSISHPRLSSSKISQLWTVNNAAGVDADENLPEWA
Celegans  no alignment  C18H9.3  n/a
Xtropicalis  no alignment  ENSXETG00000013890  n/a
protein features
start (aa)end (aa)featuredetails 
370370MOD_RESPhosphothreonine.might get lost (downstream of altered splice site)
373373MOD_RESPhosphothreonine.might get lost (downstream of altered splice site)
376376MOD_RESPhosphoserine.might get lost (downstream of altered splice site)
382382MOD_RESPhosphothreonine.might get lost (downstream of altered splice site)
436473COMPBIASPro-rich.might get lost (downstream of altered splice site)
533581DOMAINGYF.might get lost (downstream of altered splice site)
547563REGIONRequired for GRB10-binding (By similarity).might get lost (downstream of altered splice site)
593593MOD_RESPhosphoserine.might get lost (downstream of altered splice site)
6071025COMPBIASGln-rich.might get lost (downstream of altered splice site)
738888COMPBIASGlu-rich.might get lost (downstream of altered splice site)
792792CONFLICTE -> G (in Ref. 5; CAD98095).might get lost (downstream of altered splice site)
11531153CONFLICTD -> G (in Ref. 5; CAD98095).might get lost (downstream of altered splice site)
11981252COMPBIASGln-rich.might get lost (downstream of altered splice site)
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 3900 / 3900
position (AA) of stopcodon in wt / mu AA sequence 1300 / 1300
position of stopcodon in wt / mu cDNA 4095 / 4095
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 196 / 196
chromosome 2
strand 1
last intron/exon boundary 4028
theoretical NMD boundary in CDS 3782
length of CDS 3900
coding sequence (CDS) position 832
cDNA position
(for ins/del: last normal base / first normal base)		 1027
gDNA position
(for ins/del: last normal base / first normal base)		 93519
chromosomal position
(for ins/del: last normal base / first normal base)		 233655527
original gDNA sequence snippet TTCGCTCTGGCAGTGGGAGCATAGATGATGACAGGGATAGC
altered gDNA sequence snippet TTCGCTCTGGCAGTGGGAGCGTAGATGATGACAGGGATAGC
original cDNA sequence snippet TTCGCTCTGGCAGTGGGAGCATAGATGATGACAGGGATAGC
altered cDNA sequence snippet TTCGCTCTGGCAGTGGGAGCGTAGATGATGACAGGGATAGC
wildtype AA sequence MAAETQTLNF GPEWLRALSS GGSITSPPLS PALPKYKLAD YRYGREEMLA LFLKDNKIPS
DLLDKEFLPI LQEEPLPPLA LVPFTEEEQR NFSMSVNSAA VLRLTGRGGG GTVVGAPRGR
SSSRGRGRGR GECGFYQRSF DEVEGVFGRG GGREMHRSQS WEERGDRRFE KPGRKDVGRP
NFEEGGPTSV GRKHEFIRSE SENWRIFREE QNGEDEDGGW RLAGSRRDGE RWRPHSPDGP
RSAGWREHME RRRRFEFDFR DRDDERGYRR VRSGSGSIDD DRDSLPEWCL EDAEEEMGTF
DSSGAFLSLK KVQKEPIPEE QEMDFRPVDE GEECSDSEGS HNEEAKEPDK TNKKEGEKTD
RVGVEASEET PQTSSSSARP GTPSDHQSQE ASQFERKDEP KTEQTEKAEE ETRMENSLPA
KVPSRGDEMV ADVQQPLSQI PSDTASPLLI LPPPVPNPSP TLRPVETPVV GAPGMGSVST
EPDDEEGLKH LEQQAEKMVA YLQDSALDDE RLASKLQEHR AKGVSIPLMH EAMQKWYYKD
PQGEIQGPFN NQEMAEWFQA GYFTMSLLVK RACDESFQPL GDIMKMWGRV PFSPGPAPPP
HMGELDQERL TRQQELTALY QMQHLQYQQF LIQQQYAQVL AQQQKAALSS QQQQQLALLL
QQFQTLKMRI SDQNIIPSVT RSVSVPDTGS IWELQPTASQ PTVWEGGSVW DLPLDTTTPG
PALEQLQQLE KAKAAKLEQE RREAEMRAKR EEEERKRQEE LRRQQEEILR RQQEEERKRR
EEEELARRKQ EEALRRQREQ EIALRRQREE EERQQQEEAL RRLEERRREE EERRKQEELL
RKQEEEAAKW AREEEEAQRR LEENRLRMEE EAARLRHEEE ERKRKELEVQ RQKELMRQRQ
QQQEALRRLQ QQQQQQQLAQ MKLPSSSTWG QQSNTTACQS QATLSLAEIQ KLEEERERQL
REEQRRQQRE LMKALQQQQQ QQQQKLSGWG NVSKPSGTTK SLLEIQQEEA RQMQKQQQQQ
QQHQQPNRAR NNTHSNLHTS IGNSVWGSIN TGPPNQWASD LVSSIWSNAD TKNSNMGFWD
DAVKEVGPRN STNKNKNNAS LSKSVGVSNR QNKKVEEEEK LLKLFQGVNK AQDGFTQWCE
QMLHALNTAN NLDVPTFVSF LKEVESPYEV HDYIRAYLGD TSEAKEFAKQ FLERRAKQKA
NQQRQQQQLP QQQQQQPPQQ PPQQPQQQDS VWGMNHSTLH SVFQTNQSNN QQSNFEAVQS
GKKKKKQKMV RADPSLLGFS VNASSERLNM GEIETLDDY*
mutated AA sequence MAAETQTLNF GPEWLRALSS GGSITSPPLS PALPKYKLAD YRYGREEMLA LFLKDNKIPS
DLLDKEFLPI LQEEPLPPLA LVPFTEEEQR NFSMSVNSAA VLRLTGRGGG GTVVGAPRGR
SSSRGRGRGR GECGFYQRSF DEVEGVFGRG GGREMHRSQS WEERGDRRFE KPGRKDVGRP
NFEEGGPTSV GRKHEFIRSE SENWRIFREE QNGEDEDGGW RLAGSRRDGE RWRPHSPDGP
RSAGWREHME RRRRFEFDFR DRDDERGYRR VRSGSGSVDD DRDSLPEWCL EDAEEEMGTF
DSSGAFLSLK KVQKEPIPEE QEMDFRPVDE GEECSDSEGS HNEEAKEPDK TNKKEGEKTD
RVGVEASEET PQTSSSSARP GTPSDHQSQE ASQFERKDEP KTEQTEKAEE ETRMENSLPA
KVPSRGDEMV ADVQQPLSQI PSDTASPLLI LPPPVPNPSP TLRPVETPVV GAPGMGSVST
EPDDEEGLKH LEQQAEKMVA YLQDSALDDE RLASKLQEHR AKGVSIPLMH EAMQKWYYKD
PQGEIQGPFN NQEMAEWFQA GYFTMSLLVK RACDESFQPL GDIMKMWGRV PFSPGPAPPP
HMGELDQERL TRQQELTALY QMQHLQYQQF LIQQQYAQVL AQQQKAALSS QQQQQLALLL
QQFQTLKMRI SDQNIIPSVT RSVSVPDTGS IWELQPTASQ PTVWEGGSVW DLPLDTTTPG
PALEQLQQLE KAKAAKLEQE RREAEMRAKR EEEERKRQEE LRRQQEEILR RQQEEERKRR
EEEELARRKQ EEALRRQREQ EIALRRQREE EERQQQEEAL RRLEERRREE EERRKQEELL
RKQEEEAAKW AREEEEAQRR LEENRLRMEE EAARLRHEEE ERKRKELEVQ RQKELMRQRQ
QQQEALRRLQ QQQQQQQLAQ MKLPSSSTWG QQSNTTACQS QATLSLAEIQ KLEEERERQL
REEQRRQQRE LMKALQQQQQ QQQQKLSGWG NVSKPSGTTK SLLEIQQEEA RQMQKQQQQQ
QQHQQPNRAR NNTHSNLHTS IGNSVWGSIN TGPPNQWASD LVSSIWSNAD TKNSNMGFWD
DAVKEVGPRN STNKNKNNAS LSKSVGVSNR QNKKVEEEEK LLKLFQGVNK AQDGFTQWCE
QMLHALNTAN NLDVPTFVSF LKEVESPYEV HDYIRAYLGD TSEAKEFAKQ FLERRAKQKA
NQQRQQQQLP QQQQQQPPQQ PPQQPQQQDS VWGMNHSTLH SVFQTNQSNN QQSNFEAVQS
GKKKKKQKMV RADPSLLGFS VNASSERLNM GEIETLDDY*
speed 0.77 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