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 | MAF: < 0.01 (A)
Location

Chromosome 19:40397250 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM011005

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 13367, 2010_April_001_088_PRX_605725_0003

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

19:g.40397250G>A
ENST00000291825.8:c.*1307C>T
ENST00000324001.7:c.1102C>T
ENSP00000326018.6:p.Arg368Ter
LRG_265:g.21115C>T
LRG_265t2.1:c.1102C>T
LRG_265p2.1:p.Arg368Ter
LRG_265t1.1:c.*1307C>T

Variation displays