Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.16 (T)
Location

Chromosome 16:31325567 (forward strand) | View in location tab

Co-located

with COSMIC COSM3736142 (C/T) ; HGMD-PUBLIC CM0911102

Most severe consequence
Evidence status

This variation has 5 synonyms - click the plus to show

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

16:g.31325567C>T
ENST00000287497.11:c.2573C>T
ENSP00000287497.8:p.Ala858Val
ENST00000561838.1:n.389C>T
ENST00000544665.6:c.2576C>T
ENSP00000441691.2:p.Ala859Val

This variation has assays on 14 chips - click the plus to show

About this variant

This variant overlaps 7 transcripts, has 3987 individual genotypes and is mentioned in 6 citations.

Variation displays