Yum, tasty mutations...

mutation t@sting

documentation

Prediction

polymorphism

Model: without_aae, prob: 0.999998239236368 (classification due to TGP/ExAC, real probability is shown anyway)      (explain)
Summary
  • homozygous in TGP or ExAC
  • splice site changes
hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr9:18950787G>AN/A show variant in all transcripts   IGV
HGNC symbol SAXO1
Ensembl transcript ID ENST00000542071
Genbank transcript ID N/A
UniProt peptide Q8IYX7
alteration type single base exchange
alteration region 5'UTR
DNA changes cDNA.532C>T
g.82465C>T
AA changes N/A
position(s) of altered AA
if AA alteration in CDS
N/A
frameshift N/A
known variant Reference ID: rs6475273
databasehomozygous (A/A)heterozygousallele carriers
1000G14708672337
ExAC---
regulatory features H3K27me3, Histone, Histone 3 Lysine 27 Tri-Methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)0.0740
-0.1450.002
(flanking)0.2490.027
explain score(s) and/or inspect your position(s) in in UCSC Genome Browser
splice sites splice site change before start ATG (at aa -63) |
effectgDNA positionscoredetection sequence  exon-intron border
Donor gained824580.46mu: TACCAGAAAGGGTCT CCAG|aaag
distance from splice site 32
Kozak consensus sequence altered? no
conservation
protein level for non-synonymous changes
N/A
protein features no protein features affected
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 719 / 719
chromosome 9
strand -1
last intron/exon boundary 564
theoretical NMD boundary in CDS cannot be calculated, too little distance between start ATG and last intron/exon boundary
length of CDS 849
coding sequence (CDS) position N/A
cDNA position
(for ins/del: last normal base / first normal base)
532
gDNA position
(for ins/del: last normal base / first normal base)
82465
chromosomal position
(for ins/del: last normal base / first normal base)
18950787
original gDNA sequence snippet GGCGGGAGTACCAGAAAGGGCCTATACCAATGGAAGGCCTG
altered gDNA sequence snippet GGCGGGAGTACCAGAAAGGGTCTATACCAATGGAAGGCCTG
original cDNA sequence snippet GGCGGGAGTACCAGAAAGGGCCTATACCAATGGAAGGCCTG
altered cDNA sequence snippet GGCGGGAGTACCAGAAAGGGTCTATACCAATGGAAGGCCTG
wildtype AA sequence MPKLCNIPLE DVTNYKMSYV AHPVEKRFVH EAEKFRPCEI PFESLTTQKQ SYRGLMGEPA
KSLKPLARPP GLDMPFCNTT EFRDKYQAWP MPRMFSKAPI TYVPPEDRMD LLTTVQAHYT
CPKGAPAQSC RPALQIKKCG RFEGSSTTKD DYKQWSSMRT EPVKPVPQLD LPTEPLDCLT
TTRAHYVPHL PINTKSCKPH WSGPRGNVPV ESQTTYTISF TPKEMGRCLA SYPEPPGYTF
EEVDALGHRI YKPVSQAGSQ QSSHLSVDDS ENPNQRELEV LA*
mutated AA sequence N/A
speed 0.83 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