Original source

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

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

Chromosome 10:13283694 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM001301

Most severe consequence
Evidence status

Clinical significance

This variation has 4 synonyms - click the plus to show

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

10:g.13283694C>T
ENST00000396913.4:c.524G>A
ENSP00000380121.2:p.Arg175Gln
ENST00000453759.4:c.524G>A
ENSP00000412525.2:p.Arg175Gln
ENST00000396920.5:c.773G>A
ENSP00000380126.3:p.Arg258Gln
ENST00000263038.6:c.824G>A
ENSP00000263038.4:p.Arg275Gln

Variation displays