Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.01 (G)
Location

Chromosome 1:17354297 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM056695

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

1:g.17354297A>G
ENST00000475506.1:n.404T>C
ENST00000491274.1:n.494T>C
ENST00000485515.1:n.421T>C
ENST00000375499.3:c.487T>C
ENSP00000364649.3:p.Ser163Pro
ENST00000463045.1:n.649T>C
LRG_316:g.31369T>C
LRG_316t1.1:c.487T>C
LRG_316p1.1:p.Ser163Pro

This variation has assays on 4 chips - click the plus to show

Variation displays