Original source

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

Alleles
T/A | Ancestral: T | Ambiguity code: W
Location

Chromosome 8:97157401 (forward strand) | View in location tab

Most severe consequence
Clinical significance

Synonyms

LSDB 9957

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

8:g.97157401T>A
ENST00000287020.5:c.758A>T
ENSP00000287020.4:p.Gln253Leu

Variation displays