Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

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

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

Co-located

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

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, is associated with 2 phenotypes and is mentioned in 1 citation.

Variation displays