Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K
Location

Chromosome 18:21119787 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM971073

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

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

18:g.21119787T>G
ENST00000591075.1:n.76A>C
ENST00000586718.1:n.574A>C
ENST00000540608.1:n.2697A>C
ENST00000269228.5:c.2783A>C
ENSP00000269228.4:p.Gln928Pro
ENST00000412552.2:c.1829A>C
ENSP00000408606.2:p.Gln610Pro
ENST00000591051.1:c.1861A>C
ENSP00000467636.1:p.Gln621Pro

Variation displays