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 19:43511455 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM077533, CM040420

Most severe consequence
Evidence status

Clinical significance

This variation has 2 synonyms - click the plus to show

This variation has 7 HGVS names - click the plus to show

19:g.43511455G>A
ENST00000292147.4:c.487C>T
ENSP00000292147.1:p.Arg163Trp
ENST00000594342.3:c.*50C>T
ENST00000598330.1:c.*50C>T
ENST00000600651.3:c.487C>T
ENSP00000469037.1:p.Arg163Trp

Variation displays