Original source

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

Alleles
C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.07 (T)
Location

Chromosome 15:88855708 (forward strand) | View in location tab

Co-located

with COSMIC COSM3678483 (C/A), COSM3678484 (C/A)

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs11633195

This variation has 6 HGVS names - click the plus to show

About this variant

This variant overlaps 7 transcripts and has 2505 individual genotypes.

Variation displays