Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: < 0.01 (T)
Location

Chromosome 2:71668784 (forward strand) | View in location tab

Co-located

with COSMIC COSM107021 (C/T), COSM3583057 (C/T)

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB NC_000002.10:g.71749422C>T

This variant has 24 HGVS names - click the plus to show

About this variant

This variant overlaps 12 transcripts, has 2504 sample genotypes, is associated with 1 phenotype and is mentioned in 1 citation.

Somatic mutation displays