Original source

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

Alleles
C/G/T | Ancestral: C | Ambiguity code: B
Location

Chromosome 1:173873148 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM880011, CM890018

Most severe consequence
Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 6 HGVS names - click the plus to show

Variant allele T
1:g.173873148C>T
ENST00000367698.3:c.1274G>A
ENSP00000356671.3:p.Arg425His

Variant allele G
1:g.173873148C>G
ENST00000367698.3:c.1274G>C
ENSP00000356671.3:p.Arg425Pro

Variation displays