ClinVar Miner

List of variants reported as pathogenic for gastric cancer by Juno Genomics, Hangzhou Juno Genomics, Inc

Included ClinVar conditions (25):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 10
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HGVS dbSNP gnomAD frequency
NM_000038.6(APC):c.646C>T (p.Arg216Ter) rs62619935 0.00001
NM_001048174.2(MUTYH):c.773G>A (p.Gly258Glu) rs730881833 0.00001
NM_004360.5(CDH1):c.1003C>T (p.Arg335Ter) rs587780784 0.00001
NM_000038.6(APC):c.1380del (p.Glu461fs)
NM_000038.6(APC):c.1779G>A (p.Trp593Ter) rs1554083132
NM_000038.6(APC):c.3927_3931del (p.Glu1309fs) rs121913224
NM_000141.5(FGFR2):c.1025G>A (p.Cys342Tyr) rs121918487
NM_000141.5(FGFR2):c.755C>G (p.Ser252Trp) rs79184941
NM_000141.5(FGFR2):c.940-2A>G rs1057519041
NM_004985.5(KRAS):c.35G>C (p.Gly12Ala) rs121913529

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