Original source

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

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

Chromosome 3:165773492 (forward strand) | View in location tab

Co-located

with COSMIC COSM3759860 (C/T) ; HGMD-PUBLIC CM920127

Most severe consequence
Evidence status

Clinical significance

This variation has 8 synonyms - click the plus to show

This variation has 7 HGVS names - click the plus to show

3:g.165773492C>T
ENST00000482958.1:c.*205G>A
ENST00000264381.5:c.1699G>A
ENSP00000264381.3:p.Ala567Thr
ENST00000479451.3:c.289G>A
ENSP00000418325.1:p.Ala97Thr
ENST00000497011.3:c.*89G>A

This variation has assays on 9 chips - click the plus to show

Variation displays