Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
C/T|Ancestral: C|Ambiguity code: Y|MAF: < 0.01 (T)
Location

Chromosome 2:71668784 (forward strand)|View in location tab

Co-located variants
Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB NC_000002.10:g.71749422C>T

HGVS names

This variant has 24 HGVS names - Show

About this variant

This variant overlaps 12 transcripts, has 2504 sample genotypes and is mentioned in 1 citation.

Somatic mutation displays