Original source

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

Alleles
T/A | Ancestral: T | Ambiguity code: W
Location

Chromosome 1:229431830 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM043254 ; PhenCode ACTA1:c.881A>T (T/A)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NM_001100.3:c.881A>T

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

1:g.229431830T>A
ENST00000366683.3:c.512A>T
ENSP00000355644.3:p.Asp171Val
ENST00000366684.5:c.881A>T
ENSP00000355645.3:p.Asp294Val

Variation displays