Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

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

Chromosome 3:165491280 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM920127

Most severe consequence
Evidence status

Clinical significance

This variation has 8 synonyms - click the plus to show

This variation has 9 HGVS names - click the plus to show

3:g.165491280C>T
ENST00000482958.1:c.*205G>A
ENST00000264381.3:c.1699G>A
ENSP00000264381.3:p.Ala567Thr
ENST00000540653.1:c.85G>A
ENSP00000443583.1:p.Ala29Thr
ENST00000479451.1:c.289G>A
ENSP00000418325.1:p.Ala97Thr
ENST00000497011.1:c.*89G>A

This variation has assays on 8 chips - click the plus to show

Variation displays