Original source

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

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

Chromosome 4:55141018 (forward strand) | View in location tab

Co-located

with COSMIC COSM133645 (A/G) ; HGMD-PUBLIC CM066164

Most severe consequence
Clinical significance

Synonyms

LSDB 4750

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

4:g.55141018A>G
ENST00000509490.1:c.1664A>G
ENSP00000424218.1:p.Tyr555Cys
ENST00000509092.1:n.1482A>G
ENST00000507166.1:c.1018-74A>G
ENST00000257290.5:c.1664A>G
ENSP00000257290.5:p.Tyr555Cys

Variation displays