Yum, tasty mutations...

mutation t@sting

documentation

Prediction

disease causing

Model: simple_aae, prob: 0.726784450664775      (explain)
Summary
  • amino acid sequence changed
  • known as potential disease variant: rs1746 (probable pathogenic)
  • known disease mutation at this position (HGMD CM051061)
hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr11:59611471G>AN/A show variant in all transcripts   IGV
HGNC symbol CBLIF
Ensembl transcript ID ENST00000541311
Genbank transcript ID N/A
UniProt peptide P27352
alteration type single base exchange
alteration region CDS
DNA changes c.62C>T
cDNA.297C>T
g.1504C>T
AA changes S21L Score: 145 explain score(s)
position(s) of altered AA
if AA alteration in CDS
21
frameshift no
known variant Reference ID: rs121434322
databasehomozygous (A/A)heterozygousallele carriers
1000G---
ExAC01414

known as potential disease variant: rs1746 (probable pathogenic for Intrinsic factor deficiency) dbSNP  NCBI variation viewer
known disease mutation at this position, please check HGMD for details (HGMD ID CM051061)

known disease mutation at this position, please check HGMD for details (HGMD ID CM051061)
known disease mutation at this position, please check HGMD for details (HGMD ID CM051061)
regulatory features N/A
phyloP / phastCons
PhyloPPhastCons
(flanking)-4.5050.007
3.2060.657
(flanking)2.6970.665
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 58
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      21LVNGIQVLMENSVTSSAYPNPSIL
mutated  not conserved    21LVNGIQVLMENLVTSSAYPNPSI
Ptroglodytes  all identical  ENSPTRG00000003701  46LVNGIQVLMENSVTSSAYPNPSI
Mmulatta  all identical  ENSMMUG00000013523  46LVNGIQVLMENSVTSSAYPNPSI
Fcatus  all identical  ENSFCAG00000007542  46LVNGIQVLMENSVTSSAFPNPSI
Mmusculus  all identical  ENSMUSG00000024682  46WVDGLQALMENSVTDSDFPNPSI
Ggallus  no homologue    
Trubripes  no homologue    
Drerio  no homologue    
Dmelanogaster  no homologue    
Celegans  no homologue    
Xtropicalis  all conserved  ENSXETG00000025742  42LVTALLVNLERTVEANSPPDPSV
protein features no protein features affected
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 1179 / 1179
position (AA) of stopcodon in wt / mu AA sequence 393 / 393
position of stopcodon in wt / mu cDNA 1414 / 1414
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 236 / 236
chromosome 11
strand -1
last intron/exon boundary 1353
theoretical NMD boundary in CDS 1067
length of CDS 1179
coding sequence (CDS) position 62
cDNA position
(for ins/del: last normal base / first normal base)
297
gDNA position
(for ins/del: last normal base / first normal base)
1504
chromosomal position
(for ins/del: last normal base / first normal base)
59611471
original gDNA sequence snippet ACAAGTACTCATGGAGAACTCGGTGACTTCATCAGCCTACC
altered gDNA sequence snippet ACAAGTACTCATGGAGAACTTGGTGACTTCATCAGCCTACC
original cDNA sequence snippet ACAAGTACTCATGGAGAACTCGGTGACTTCATCAGCCTACC
altered cDNA sequence snippet ACAAGTACTCATGGAGAACTTGGTGACTTCATCAGCCTACC
wildtype AA sequence MAVPSAQEPL VNGIQVLMEN SVTSSAYPNP SILIAMNLAG AYNLKAQKLL TYQLMSSDNN
DLTIGQLGLT IMALTSSCRD PGDKVSILQR QMENWAPSSP NAEASAFYGP SLAILALCQK
NSEATLPIAV RFAKTLLANS SPFNVDTGAM ATLALTCMYN KIPVGSEEGY RSLFGQVLKD
IVEKISMKIK DNGIIGDIYS TGLAMQALSV TPEPSKKEWN CKKTTDMILN EIKQGKFHNP
MSIAQILPSL KGKTYLDVPQ VTCSPDHEVQ PTLPSNPGPG PTSASNITVI YTINNQLRGV
ELLFNETINV SVKSGSVLLV VLEEAQRKNP MFKFETTMTS WGLVVSSINN IAENVNHKTY
WQFLSGVTPL NEGVADYIPF NHEHITANFT QY*
mutated AA sequence MAVPSAQEPL VNGIQVLMEN LVTSSAYPNP SILIAMNLAG AYNLKAQKLL TYQLMSSDNN
DLTIGQLGLT IMALTSSCRD PGDKVSILQR QMENWAPSSP NAEASAFYGP SLAILALCQK
NSEATLPIAV RFAKTLLANS SPFNVDTGAM ATLALTCMYN KIPVGSEEGY RSLFGQVLKD
IVEKISMKIK DNGIIGDIYS TGLAMQALSV TPEPSKKEWN CKKTTDMILN EIKQGKFHNP
MSIAQILPSL KGKTYLDVPQ VTCSPDHEVQ PTLPSNPGPG PTSASNITVI YTINNQLRGV
ELLFNETINV SVKSGSVLLV VLEEAQRKNP MFKFETTMTS WGLVVSSINN IAENVNHKTY
WQFLSGVTPL NEGVADYIPF NHEHITANFT QY*
speed 1.18 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