Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.29 (C)
Location

Chromosome 1:50666515 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 2 synonyms - click the plus to show

This variation has 10 HGVS names - click the plus to show

1:g.50666515C>T
ENST00000371824.1:c.774-8C>T
ENST00000448907.2:c.783-8C>T
ENST00000371821.1:c.823C>T
ENSP00000360886.1:p.Pro275Ser
ENST00000371819.1:c.789-8C>T
ENST00000371827.1:c.774-8C>T
ENST00000357083.4:c.825-8C>T
ENST00000371823.4:c.808C>T
ENSP00000360888.4:p.Pro270Ser

This variation has assays on 4 chips - click the plus to show

Variation displays