Original source

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

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

Chromosome 4:185144963 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM020975

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

4:g.185144963A>G
ENST00000491736.1:c.311A>G
ENSP00000476711.1:p.Asp104Gly
ENST00000281456.8:c.311A>G
ENSP00000281456.5:p.Asp104Gly

Variation displays