Original source

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

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

Chromosome 18:21119905 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM990944

Most severe consequence
Clinical significance

Synonyms

LSDB 15109

This variation has 9 HGVS names - click the plus to show

18:g.21119905C>T
ENST00000586718.1:n.456G>A
ENST00000540608.1:n.2579G>A
ENST00000269228.5:c.2665G>A
ENSP00000269228.4:p.Val889Met
ENST00000412552.2:c.1711G>A
ENSP00000408606.2:p.Val571Met
ENST00000591051.1:c.1743G>A
ENSP00000467636.1:p.Val582Met

Variation displays