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 1:92149333 (forward strand) | View in location tab

Co-located

with COSMIC COSM1179616 (G/A)

Most severe consequence
Evidence status

Synonyms

LSDB NM_003243.4:c.2519C>T

This variation has 11 HGVS names - click the plus to show

Variation displays