Original source

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

G/A | Ancestral: G | Ambiguity code: R

Chromosome 17:37880997 (forward strand) | View in location tab


with COSMIC COSM685 (G/A), COSM19875 (G/TTGT), COSM12554 (G/CTTT), COSM20895 (G/TTAT), COSM303938 (G/T) ; dbSNP_ClinVar rs397516980 (G/TTAT)

Most severe consequence
Evidence status

Clinical significance

This variation has 4 synonyms - click the plus to show

This variation has 19 HGVS names - click the plus to show

Variation displays