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 18:23538651 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM012436

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

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

18:g.23538651G>A
ENST00000591075.1:n.565C>T
ENST00000269228.7:c.2932C>T
ENSP00000269228.4:p.Arg978Cys
ENST00000591955.1:n.275C>T
ENST00000591051.1:c.2010C>T
ENSP00000467636.1:p.Arg671Cys

Variation displays