Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.30 (A)
Location

Chromosome 16:88646828 (forward strand) | View in location tab

Co-located

with COSMIC COSM3755197 (A/G) ; HGMD-PUBLIC CM983302

Most severe consequence
Evidence status

Clinical significance

This variation has 10 synonyms - click the plus to show

This variation has 17 HGVS names - click the plus to show

16:g.88646828A>G
ENST00000563526.3:n.189T>C
ENST00000567174.3:c.214T>C
ENSP00000454951.1:p.Tyr72His
ENST00000568278.1:c.214T>C
ENSP00000455506.1:p.Tyr72His
ENST00000566229.1:c.203T>C
ENSP00000457060.1:p.Val68Ala
ENST00000569359.3:c.214T>C
ENSP00000456079.1:p.Tyr72His
ENST00000261623.5:c.214T>C
ENSP00000261623.3:p.Tyr72His
ENST00000562209.1:n.494T>C
ENST00000566534.3:n.236T>C
LRG_52:g.9222T>C
LRG_52t1:c.214T>C
LRG_52p1:p.Tyr72His

This variation has assays on 11 chips - click the plus to show

Variation displays