This variation has been flagged

Variation has more than 3 different alleles

Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

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

Chromosome 7:55174014 (forward strand) | View in location tab


with COSMIC COSM6253 (G/T), COSM6252 (G/A)

Most severe consequence
Evidence status

Clinical significance

This variation has 6 synonyms - click the plus to show

This variation has 33 HGVS names - click the plus to show

About this variant

This variant overlaps 18 transcripts, is associated with 7 phenotypes and is mentioned in 1 citation.

Variation displays