This variation has been flagged

Variation has more than 3 different alleles

Original source

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

Alleles
C/A/G/T | Ancestral: C | Ambiguity code: N
Location

Chromosome 3:41266137 (forward strand) | View in location tab

Co-located

with COSMIC COSM5689 (C/G), COSM5692 (C/A), COSM5667 (C/T), COSM6100 (C/-)

Most severe consequence
Evidence status

Clinical significance

This variation has 7 synonyms - click the plus to show

This variation has 60 HGVS names - click the plus to show

Variation displays