Original source

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

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

Chromosome 1:98348885 (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 7 HGVS names - click the plus to show

1:g.98348885G>A
ENST00000423006.2:c.39+37555C>T
ENST00000306031.5:c.85C>T
ENSP00000307107.5:p.Arg29Cys
ENST00000370192.3:c.85C>T
ENSP00000359211.3:p.Arg29Cys
ENST00000460019.1:n.160C>T

This variation has assays on 10 chips - click the plus to show

Variation displays