Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
C/T | Ambiguity code: Y | MAF: 0.11 (T)
Location

Chromosome 5:96786506 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 4 synonyms - click the plus to show

This variation has 7 HGVS names - click the plus to show

5:g.96786506C>T
ENST00000443439.5:c.1723G>A
ENSP00000406304.2:p.Asp575Asn
ENST00000507859.1:n.386G>A
ENST00000514604.4:n.147G>A
ENST00000296754.6:c.1723G>A
ENSP00000296754.3:p.Asp575Asn

This variation has assays on 13 chips - click the plus to show

About this variant

This variant overlaps 7 transcripts, has 2647 individual genotypes and is mentioned in 19 citations.

Variation displays