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 8:86632768 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM001816

Most severe consequence
Clinical significance

Synonyms

LSDB 12958

This variation has 3 HGVS names - click the plus to show

8:g.86632768G>A
ENST00000320005.5:c.1304C>T
ENSP00000316605.5:p.Ser435Phe

Variation displays