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 | MAF: < 0.01 (T)
Location

Chromosome 10:71570884 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM074087

Most severe consequence
Evidence status

Clinical significance

This variation has 2 synonyms - click the plus to show

This variation has 17 HGVS names - click the plus to show

10:g.71570884C>T
ENST00000616684.2:c.854C>T
ENSP00000482036.1:p.Pro285Leu
ENST00000622827.2:c.719C>T
ENSP00000483211.1:p.Pro240Leu
ENST00000466757.5:c.90C>T
ENSP00000473539.1:p.Pro31Leu
ENST00000398842.5:c.470C>T
ENSP00000381822.4:p.Pro157Leu
ENST00000299366.9:c.854C>T
ENSP00000299366.7:p.Pro285Leu
ENST00000398809.6:c.719C>T
ENSP00000381789.5:p.Pro240Leu
ENST00000461841.5:c.854C>T
ENSP00000473454.1:p.Pro285Leu
ENST00000224721.8:c.869C>T
ENSP00000224721.7:p.Pro290Leu

Genotyping chips

This variation has assays on: HumanCoreExome-12

Variation displays