Original source

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

Alleles
G/A/T | Ancestral: G | Ambiguity code: D
Location

Chromosome 1:173883864 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM860005, CM930047

Most severe consequence
Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 8 HGVS names - click the plus to show

Variant allele A
1:g.173883864G>A
ENST00000494024.1:n.461C>T
ENST00000367698.3:c.235C>T
ENSP00000356671.3:p.Arg79Cys

Variant allele T
1:g.173883864G>T
ENST00000494024.1:n.461C>A
ENST00000367698.3:c.235C>A
ENSP00000356671.3:p.Arg79Ser

Variation displays