Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.11 (A)
Location

Chromosome 10:13298236 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM001290

Most severe consequence
Evidence status

Clinical significance

This variation has 2 synonyms - click the plus to show

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

10:g.13298236G>A
ENST00000463730.1:n.140C>T
ENST00000396913.3:c.-167+1184C>T
ENST00000453759.3:c.-216C>T
ENST00000396920.4:c.28C>T
ENSP00000380126.3:p.Pro10Ser
ENST00000263038.5:c.85C>T
ENSP00000263038.4:p.Pro29Ser
ENST00000479604.1:c.85C>T
ENSP00000420117.1:p.Pro29Ser

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

Variation displays