Original source

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

Alleles
A/C | Ancestral: A | Ambiguity code: M
Location

Chromosome 10:93797277 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM020460

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 4 HGVS names - click the plus to show

10:g.93797277A>C
ENST00000371413.3:c.839-472A>C
ENST00000371418.5:c.1148A>C
ENSP00000360472.4:p.Glu383Ala

Variation displays