List of variants in gene combination DHFR, MSH3 reported as likely pathogenic for female reproductive organ cancer

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_002439.5(MSH3):c.136C>T (p.Gln46Ter)	rs779180469	0.00001
NM_002439.5(MSH3):c.237+2T>C	rs1480047980	0.00001
NM_002439.5(MSH3):c.76C>T (p.Arg26Ter)	rs770190473	0.00001
NM_002439.5(MSH3):c.131_138del (p.Ala44fs)	rs2112797412
NM_002439.5(MSH3):c.146del (p.Pro49fs)	rs1580538168
NM_002439.5(MSH3):c.14del (p.Lys5fs)	rs1749186228
NM_002439.5(MSH3):c.15del (p.Lys5fs)
NM_002439.5(MSH3):c.161del (p.Ala54fs)
NM_002439.5(MSH3):c.169_196del (p.Ala57fs)
NM_002439.5(MSH3):c.200dup (p.Ala68fs)
NM_002439.5(MSH3):c.211_218dup (p.Gln74fs)
NM_002439.5(MSH3):c.211_230dup (p.His78fs)	rs1749219575
NM_002439.5(MSH3):c.215del (p.Pro72fs)
NM_002439.5(MSH3):c.220C>T (p.Gln74Ter)
NM_002439.5(MSH3):c.96delinsCT (p.Gly32_Ser33insTer)

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