View genomic variant #0000023579

Chromosome 1
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.45796220C>T
Published as -
GERP -
Segregation -
DB-ID MUTYH_000001
MSCV -
dbSNP ID -
Frequency -
Sources ;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) Variant not found in online data sets
Owner Lishuang Shen




Variant on transcripts

6 entries on 1 page. Showing entries 1 - 6.
Legend  

Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
MUTYH 00000923 NM_001048171.1 0000023579 ./. - - c.1444G>A p.(Val482Met) - - - -
MUTYH 00000927 NM_001048172.1 0000023579 ./. - - c.1405G>A p.(Val469Met) - - - -
MUTYH 00000926 NM_001048173.1 0000023579 ./. - - c.1402G>A p.(Val468Met) - - - -
MUTYH 00000928 NM_001048174.1 0000023579 ./. - - c.1402G>A p.(Val468Met) - - - -
MUTYH 00000925 NM_001128425.1 0000023579 ./. - - c.1486G>A p.(Val496Met) - - - -
MUTYH 00000924 NM_012222.2 0000023579 ./. - - c.1477G>A p.(Val493Met) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000129217; RCV000226351;
Chromosome 1:45796220..45796220
ClinVar Allele ID 150656
Disease database name and identifier MONDO:MONDO:0015356, MeSH:D009386, MedGen:C0027672, Orphanet:140162|MONDO:MONDO:0012041, MedGen:C3272841, OMIM:608456, Orphanet:220460, Orphanet:247798
ClinVar preferred disease name Hereditary cancer-predisposing syndrome|Familial adenomatous polyposis 2
HGVS variant names NC 000001.10:g.45796220C>T
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Uncertain significance
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA012933
Gene symbol:Gene id. MUTYH:4595
Molecular consequence SO:0001583|missense variant, SO:0001619|non-coding transcript variant
Allele origin germline
dbSNP ID 587781385
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

None

Ensembl Variant Phenotype Information:

None