Original source

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

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

Chromosome 8:43193824 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM065253

Most severe consequence
Clinical significance

Synonyms

LSDB 16746

This variation has 8 HGVS names - click the plus to show

8:g.43193824T>A
ENST00000521576.1:c.596T>A
ENSP00000429029.1:p.Met199Lys
ENST00000520678.1:n.378T>A
ENST00000379644.6:c.1445T>A
ENSP00000368965.4:p.Met482Lys
ENST00000524016.3:c.549T>A
ENSP00000428322.1:p.Met184Lys

Variation displays