List of variants in gene combination ATM, C11orf65 reported as likely pathogenic for Malignant tumor of breast

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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: 8

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HGVS	dbSNP	gnomAD frequency
NM_000051.4(ATM):c.9023G>A (p.Arg3008His)	rs587781894	0.00001
NM_000051.4(ATM):c.6200C>A (p.Ala2067Asp)	rs397514577
NM_000051.4(ATM):c.6273del (p.Trp2091fs)	rs1565503137
NM_000051.4(ATM):c.7311C>A (p.Tyr2437Ter)	rs763470424
NM_000051.4(ATM):c.8268+1G>T	rs876658957
NM_000051.4(ATM):c.8418+5G>A	rs1305740166
NM_000051.4(ATM):c.8584+1G>C	rs876658182
NM_000051.4(ATM):c.8671+1G>T	rs1555139694

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