Original source

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

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

Chromosome 17:7675214 (forward strand) | View in location tab


with COSMIC COSM1640870 (A/G), COSM437607 (A/T), COSM1559497 (A/C), COSM1640868 (A/G), COSM3388221 (A/C), COSM3388222 (A/C), COSM3712458 (A/G), COSM437608 (A/T), COSM1640871 (A/G), COSM1559498 (A/C), COSM1640869 (A/G), COSM1559496 (A/C), COSM437606 (A/T), COSM437605 (A/T), COSM1559495 (A/C), COSM1640867 (A/G), COSM43730 (A/C), COSM11781 (A/T), COSM132890 (A/-), COSM43723 (A/G) ; HGMD-PUBLIC CM973400, CM910373 ; PhenCode TP53_g.12386T>A (A/T), TP53_g.12386T>C (A/G), TP53_g.12386T>G (A/C)

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 73 HGVS names - click the plus to show

About this variant

This variant overlaps 42 transcripts and is associated with 3 phenotypes.

Variation displays