Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 3:57232305 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM980971

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 5 HGVS names - click the plus to show

3:g.57232305G>A
ENST00000473921.1:c.376C>T
ENSP00000418918.1:p.Arg126Cys
ENST00000295934.3:c.478C>T
ENSP00000295934.3:p.Arg160Cys

Variation displays