Original source

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

Alleles
C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.43 (T)
Location

Chromosome 15:88855879 (forward strand) | View in location tab

Co-located

with COSMIC COSM4128542 (C/T)

Most severe consequence
 
Synonymous variant
Evidence status

Synonyms

Archive dbSNP rs71408892, rs71408893

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

About this variant

This variant overlaps 7 transcripts and has 2508 sample genotypes.

Variant displays