Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.29 (A)
Location

Chromosome 16:88643420 (forward strand) | View in location tab

Co-located

with COSMIC COSM3749388 (A/G)

Most severe consequence
Evidence status

This variation has 6 synonyms - click the plus to show

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

16:g.88643420A>G
ENST00000261623.5:c.521T>C
ENSP00000261623.3:p.Val174Ala
LRG_52:g.12630T>C
LRG_52t1:c.521T>C
LRG_52p1:p.Val174Ala

Genotyping chips

This variation has assays on: Illumina_ExomeChip

Variation displays