Original source

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

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

Chromosome 1:229431633 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM043255 ; PhenCode ACTA1:c.1000C>T (G/A)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NM_001100.3:c.1000C>T

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

1:g.229431633G>A
ENST00000366683.3:c.631C>T
ENSP00000355644.3:p.Pro211Ser
ENST00000366684.5:c.1000C>T
ENSP00000355645.3:p.Pro334Ser

Variation displays