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

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

Chromosome X:70339254 (forward strand) | View in location tab


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

Most severe consequence

This variation has 5 synonyms - click the plus to show

This variation has 27 HGVS names - click the plus to show

Variation displays