Original source

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

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

Chromosome 17:39724744 (forward strand) | View in location tab


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

Most severe consequence
Evidence status

Clinical significance

This variation has 4 synonyms - click the plus to show

This variation has 17 HGVS names - click the plus to show

About this variant

This variant overlaps 20 transcripts, is associated with 3 phenotypes and is mentioned in 1 citation.

Variation displays