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/C/T | Ambiguity code: N

Chromosome X:71119404 (forward strand) | View in location tab


with COSMIC COSM131595 (G/C), COSM131596 (G/A), COSM131597 (G/T), COSM213674 (G/A), COSM1736588 (G/C), COSM4169328 (G/A), COSM3786773 (G/C)

Most severe consequence
Clinical significance

This variation has 5 synonyms - click the plus to show

This variation has 24 HGVS names - click the plus to show

Variation displays