Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

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

Chromosome 18:23539941 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM990944

Most severe consequence
Clinical significance

Synonyms

LSDB 15109

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

18:g.23539941C>T
ENST00000586718.1:n.456G>A
ENST00000540608.3:n.2579G>A
ENST00000269228.7:c.2665G>A
ENSP00000269228.4:p.Val889Met
ENST00000591051.1:c.1743G>A
ENSP00000467636.1:p.Val582Met

Variation displays