Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: < 0.01 (A)
Location

Chromosome 5:41862758 (forward strand) | View in location tab

Most severe consequence
Evidence status

Clinical significance

This variation has 2 synonyms - click the plus to show

This variation has 3 HGVS names - click the plus to show

5:g.41862758G>A
ENST00000196371.5:c.173C>T
ENSP00000196371.5:p.Thr58Met

Genotyping chips

This variation has assays on: Illumina_ExomeChip

Variation displays