ClinVar Miner

List of variants studied for adenocarcinoma by Neuberg Centre For Genomic Medicine, NCGM

Included ClinVar conditions (112):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 3
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HGVS dbSNP gnomAD frequency
NM_020975.6(RET):c.2261C>T (p.Thr754Met) rs181856591 0.00009
NM_000245.4(MET):c.2887+1G>T
NM_020975.6(RET):c.1142T>G (p.Phe381Cys)

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