Original source

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

Alleles
C/A/G/T | Ancestral: C | Ambiguity code: N
Location

Chromosome 18:21118573 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM012438, CM012439, CM981390

Most severe consequence
Evidence status

Clinical significance

This variation has 9 synonyms - click the plus to show

This variation has 27 HGVS names - click the plus to show

Variant allele A
18:g.21118573C>A
ENST00000591075.1:n.607G>T
ENST00000591955.1:n.317G>T
ENST00000269228.5:c.2974G>T
ENSP00000269228.4:p.Gly992Trp
ENST00000412552.2:c.2020G>T
ENSP00000408606.2:p.Gly674Trp
ENST00000591051.1:c.2052G>T
ENSP00000467636.1:p.Gly685Trp

Variant allele T
18:g.21118573C>T
ENST00000591075.1:n.607G>A
ENST00000591955.1:n.317G>A
ENST00000269228.5:c.2974G>A
ENSP00000269228.4:p.Gly992Arg
ENST00000412552.2:c.2020G>A
ENSP00000408606.2:p.Gly674Arg
ENST00000591051.1:c.2052G>A
ENSP00000467636.1:p.Gly685Arg

Variant allele G
18:g.21118573C>G
ENST00000591075.1:n.607G>C
ENST00000591955.1:n.317G>C
ENST00000269228.5:c.2974G>C
ENSP00000269228.4:p.Gly992Arg
ENST00000412552.2:c.2020G>C
ENSP00000408606.2:p.Gly674Arg
ENST00000591051.1:c.2052G>C
ENSP00000467636.1:p.Gly685Arg

Variation displays