Original source

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

Alleles
A/C | Ancestral: A | Ambiguity code: M
Location

Chromosome 6:121768043 (forward strand) | View in location tab

Co-located

with COSMIC COSM161265 (A/G) ; HGMD-PUBLIC CM030451

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_060_GJA1_121014_0003, 1371

This variation has 3 HGVS names - click the plus to show

6:g.121768043A>C
ENST00000282561.3:c.50A>C
ENSP00000282561.3:p.Tyr17Ser

Variation displays