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 4:155507143 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM920272

Most severe consequence
Clinical significance

Synonyms

LSDB 1933

This variation has 5 HGVS names - click the plus to show

4:g.155507143T>A
ENST00000302053.3:c.1438A>T
ENSP00000306361.3:p.Lys480Ter
ENST00000403106.3:c.1438A>T
ENSP00000385981.3:p.Lys480Ter

Variation displays