Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 4:155510665 (forward strand) | View in location tab

Co-located

with COSMIC COSM218791 (C/T) ; HGMD-PUBLIC CM810009

Most severe consequence
Clinical significance

Synonyms

LSDB 1926

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

4:g.155510665C>T
ENST00000302053.3:c.104G>A
ENSP00000306361.3:p.Arg35His
ENST00000403106.3:c.104G>A
ENSP00000385981.3:p.Arg35His

Variation displays