Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 4:154589514 (forward strand) | View in location tab

Co-located

with COSMIC COSM294372 (G/A), COSM4122964 (G/A) ; HGMD-PUBLIC CM930249, CM100506

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 1925

This variation has 12 HGVS names - click the plus to show

4:g.154589514G>A
ENST00000302053.6:c.103C>T
ENSP00000306361.3:p.Arg35Cys
ENST00000403106.6:c.103C>T
ENSP00000385981.3:p.Arg35Cys
ENST00000622532.1:c.103C>T
ENSP00000478487.1:p.Arg35Cys
LRG_557:g.6232C>T
LRG_557t2:c.103C>T
LRG_557p2:p.Arg35Cys
LRG_557t1:c.103C>T
LRG_557p1:p.Arg35Cys

About this variant

This variant overlaps 6 transcripts and is associated with 2 phenotypes.

Variation displays