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 12:868046 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM064053

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 14 HGVS names - click the plus to show

12:g.868046C>T
ENST00000315939.8:c.2140-3219C>T
ENST00000535698.1:c.36+5776C>T
ENST00000545285.3:c.98-3219C>T
ENST00000574564.1:c.217C>T
ENSP00000460651.1:p.Gln73Ter
ENST00000530271.4:c.2320C>T
ENSP00000433548.3:p.Gln774Ter
ENST00000340908.6:c.2575C>T
ENSP00000341292.5:p.Gln859Ter
ENST00000544965.3:c.190+5776C>T
ENST00000537687.3:c.2320C>T
ENSP00000444465.1:p.Gln774Ter
ENST00000535572.3:c.2140-3219C>T

Variation displays