NM_005379.4(MYO1A):c.2887G>A (p.Val963Met)Rat Genome Database
Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   

Variant : CV171525 (NM_005379.4(MYO1A):c.2887G>A (p.Val963Met)) Homo sapiens

Symbol: CV171525
Name: NM_005379.4(MYO1A):c.2887G>A (p.Val963Met)
RGD ID: 9686949
Condition: Malignant tumor of prostate [RCV000149168]
Clinical Significance: uncertain significance
Last Evaluated:
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: MYO1A  
Variant Type: single nucleotide variant (SO:0001583)
Source: CLINVAR
Molecular Consequence: missense variant
Evidence: literature only
HGVS Name(s): NG_012104.1:g.25860G>A
NC_000012.12:g.57029250C>T
NC_000012.11:g.57423034C>T
NM_005379.2:c.2887G>A
NP_005370.1:p.Val963Met
NM_005379.4:c.2887G>A
NM_001256041.2:c.2887G>A
NP_001242970.1:p.Val963Met
Position
Human AssemblyChrPosition (strand)Source
GRCh381257,029,250 - 57,029,250CLINVAR
GRCh371257,423,034 - 57,423,034CLINVAR
Cytogenetic Map1212q13.3CLINVAR
Trait Synonyms: Prostate cancer; Prostatic cancer
Age Of Onset: adulthood
Prevalence: 1-9 / 100 000



Disease Annotations     Click to see Annotation Detail View


References - curated
1. RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
Additional References at PubMed
PMID:23265383  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000149168 CLINVAR
dbSNP (RS) rs193921066 CLINVAR
MedGen C0376358 CLINVAR
NCBI Gene MYO1A CLINVAR
OMIM 176807 CLINVAR
  601478 CLINVAR
SNOMED CT 399068003 CLINVAR