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 | MAF: 0.03 (T)
Location

Chromosome 9:133657152 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM054656

Most severe consequence
Evidence status

This variation has 2 synonyms - click the plus to show

This variation has 4 HGVS names - click the plus to show

9:g.133657152C>T
ENST00000393056.4:c.1645C>T
ENSP00000376776.2:p.Arg549Cys
ENST00000425189.1:n.162G>A

This variation has assays on 8 chips - click the plus to show

Variation displays