Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.23 (G)
Location

Chromosome 1:97883329 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM970421

Most severe consequence
Evidence status

Clinical significance

This variation has 7 synonyms - click the plus to show

This variation has 11 HGVS names - click the plus to show

1:g.97883329A>G
ENST00000306031.5:c.85T>C
ENSP00000307107.5:p.Cys29Arg
ENST00000370192.4:c.85T>C
ENSP00000359211.3:p.Cys29Arg
ENST00000460019.1:n.160T>C
LRG_722:g.42731T>C
LRG_722t2.1:c.85T>C
LRG_722p2.1:p.Cys29Arg
LRG_722t1.1:c.85T>C
LRG_722p1.1:p.Cys29Arg

This variation has assays on 11 chips - click the plus to show

Variation displays