Yum, tasty mutations...

mutation t@sting

 documentation

Prediction

disease causing

 Model: simple_aae, prob: 7.39880651184119e-10 (classification due to ClinVar, real probability is shown anyway)      (explain)
Summary
  • amino acid sequence changed
  • known disease mutation at this position (HGMD CM082673)
  • known disease mutation: rs9123 (pathogenic)
 hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr10:103534925A>GN/A show variant in all transcripts   IGV
HGNC symbol FGF8
Ensembl transcript ID ENST00000344255
Genbank transcript ID NM_033164
UniProt peptide P55075
alteration type single base exchange
alteration region CDS
DNA changes c.118T>C
cDNA.118T>C
g.903T>C
AA changes F40L Score: 22 explain score(s)
position(s) of altered AA
if AA alteration in CDS		 40
frameshift no
known variant Reference ID: rs137852661
Allele 'G' was neither found in ExAC nor 1000G.
known disease mutation: rs9123 (pathogenic for Hypogonadotropic hypogonadism 6 with or without anosmia) dbSNP  NCBI variation viewer
known disease mutation at this position, please check HGMD for details (HGMD ID CM082673)

known disease mutation at this position, please check HGMD for details (HGMD ID CM082673)
known disease mutation at this position, please check HGMD for details (HGMD ID CM082673)
regulatory features H3K27me3, Histone, Histone 3 Lysine 27 Tri-Methylation
H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
H3K4me2, Histone, Histone 3 Lysine 4 Di-Methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)0.4390.025
-0.6150.039
(flanking)0.840.628
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 39
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      40GPALGRELASLFRAGREPQGVSQQ
mutated  not conserved    40GPALGRELASLLRAGREPQGVSQ
Ptroglodytes  all identical  ENSPTRG00000002874  40GPALGRELASLFRAGREPQGVSQ
Mmulatta  no alignment  ENSMMUG00000015771  n/a
Fcatus  not conserved  ENSFCAG00000007177  40GAALGRELASLCGAGRESQGVSQ
Mmusculus  not conserved  ENSMUSG00000025219  40GNPADTLGQGHEDRPFGQRSRAGKN
Ggallus  not conserved  ENSGALG00000007706  43PPNF------------------T
Trubripes  no homologue    
Drerio  not conserved  ENSDARG00000003399  40PPNF------------------T
Dmelanogaster  no alignment  FBgn0014135  n/a
Celegans  no alignment  C05D11.4  n/a
Xtropicalis  not conserved  ENSXETG00000014474  40GSPTERE--GIRRESEAPRGEVSTQVTVQSPPNFT
protein features no protein features affected
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 702 / 702
position (AA) of stopcodon in wt / mu AA sequence 234 / 234
position of stopcodon in wt / mu cDNA 702 / 702
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 1 / 1
chromosome 10
strand -1
last intron/exon boundary 412
theoretical NMD boundary in CDS 361
length of CDS 702
coding sequence (CDS) position 118
cDNA position
(for ins/del: last normal base / first normal base)		 118
gDNA position
(for ins/del: last normal base / first normal base)		 903
chromosomal position
(for ins/del: last normal base / first normal base)		 103534925
original gDNA sequence snippet GCAGGGAGCTCGCTTCCCTGTTCCGGGCTGGCCGGGAGCCC
altered gDNA sequence snippet GCAGGGAGCTCGCTTCCCTGCTCCGGGCTGGCCGGGAGCCC
original cDNA sequence snippet GCAGGGAGCTCGCTTCCCTGTTCCGGGCTGGCCGGGAGCCC
altered cDNA sequence snippet GCAGGGAGCTCGCTTCCCTGCTCCGGGCTGGCCGGGAGCCC
wildtype AA sequence MGSPRSALSC LLLHLLVLCL QAQEGPGRGP ALGRELASLF RAGREPQGVS QQHVREQSLV
TDQLSRRLIR TYQLYSRTSG KHVQVLANKR INAMAEDGDP FAKLIVETDT FGSRVRVRGA
ETGLYICMNK KGKLIAKSNG KGKDCVFTEI VLENNYTALQ NAKYEGWYMA FTRKGRPRKG
SKTRQHQREV HFMKRLPRGH HTTEQSLRFE FLNYPPFTRS LRGSQRTWAP EPR*
mutated AA sequence MGSPRSALSC LLLHLLVLCL QAQEGPGRGP ALGRELASLL RAGREPQGVS QQHVREQSLV
TDQLSRRLIR TYQLYSRTSG KHVQVLANKR INAMAEDGDP FAKLIVETDT FGSRVRVRGA
ETGLYICMNK KGKLIAKSNG KGKDCVFTEI VLENNYTALQ NAKYEGWYMA FTRKGRPRKG
SKTRQHQREV HFMKRLPRGH HTTEQSLRFE FLNYPPFTRS LRGSQRTWAP EPR*
speed 0.99 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