Original source

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

Alleles
C/A/T | Ancestral: C | Ambiguity code: H
Location

Chromosome 4:155506863 (forward strand) | View in location tab

Co-located

with COSMIC COSM1579303 (C/T), COSM1637833 (C/A) ; HGMD-PUBLIC CM930250, CM0910627

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 1934

This variation has 10 HGVS names - click the plus to show

Variant allele A
4:g.155506863C>A
ENST00000302053.3:c.1718G>T
ENSP00000306361.3:p.Arg573Leu
ENST00000403106.3:c.1718G>T
ENSP00000385981.3:p.Arg573Leu

Variant allele T
4:g.155506863C>T
ENST00000302053.3:c.1718G>A
ENSP00000306361.3:p.Arg573His
ENST00000403106.3:c.1718G>A
ENSP00000385981.3:p.Arg573His

Variation displays