List of variants in gene combination ATM, C11orf65 reported as pathogenic for Breast and/or ovarian 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: 13

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HGVS	dbSNP	gnomAD frequency
NM_000051.4(ATM):c.7271T>G (p.Val2424Gly)	rs28904921	0.00006
NM_000051.4(ATM):c.5932G>T (p.Glu1978Ter)	rs587779852	0.00004
NM_000051.4(ATM):c.6807G>A (p.Gln2269=)	rs587780638	0.00001
NM_000051.4(ATM):c.8266A>T (p.Lys2756Ter)	rs371638537	0.00001
NM_000051.4(ATM):c.6096-9_6096-5del	rs879254095
NM_000051.4(ATM):c.6913C>T (p.Gln2305Ter)	rs1282099124
NM_000051.4(ATM):c.7327C>T (p.Arg2443Ter)	rs121434220
NM_000051.4(ATM):c.7638_7646del (p.Arg2547_Ser2549del)	rs587776547
NM_000051.4(ATM):c.7705_7706del (p.Arg2568_Asp2569insTer)	rs759965045
NM_000051.4(ATM):c.8140C>T (p.Gln2714Ter)	rs1060501695
NM_000051.4(ATM):c.8418+5_8418+8del	rs730881295
NM_000051.4(ATM):c.8655dup (p.Val2886fs)	rs753961188
NM_000051.4(ATM):c.8850+1G>A	rs1555143620

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