ClinVar Miner

List of variants in gene combination ATM, C11orf65 studied for Familial cancer of breast

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Total variants: 27
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HGVS dbSNP
NM_000051.3(ATM):c.5948G>A (p.Ser1983Asn) rs659243
NM_000051.3(ATM):c.6095G>A (p.Arg2032Lys) rs139770721
NM_000051.3(ATM):c.6116A>T (p.Glu2039Val) rs876659558
NM_000051.3(ATM):c.6976-2A>C rs587782403
NM_000051.3(ATM):c.7089+1G>T rs777741666
NM_000051.3(ATM):c.7271T>G (p.Val2424Gly) rs28904921
NM_000051.3(ATM):c.7327C>T (p.Arg2443Ter) rs121434220
NM_000051.3(ATM):c.7475T>G (p.Leu2492Arg) rs56399857
NM_000051.3(ATM):c.7629+2T>C rs786203059
NM_000051.3(ATM):c.7926A>C (p.Arg2642Ser) rs863224440
NM_000051.3(ATM):c.8147T>C (p.Val2716Ala) rs587782652
NM_000051.3(ATM):c.8418+5_8418+8del rs730881295
NM_000051.3(ATM):c.8711A>G (p.Glu2904Gly) rs786202826
NM_000051.3(ATM):c.8988-1G>A rs730881386
NM_000051.4(ATM):c.6215del (p.Gly2072fs)
NM_000051.4(ATM):c.6820G>A (p.Ala2274Thr) rs567060474
NM_000051.4(ATM):c.6860G>C (p.Gly2287Ala) rs1800061
NM_000051.4(ATM):c.7089+1_7089+38del
NM_000051.4(ATM):c.7751_7754del (p.Thr2584fs)
NM_000051.4(ATM):c.7879T>C (p.Tyr2627His)
NM_000051.4(ATM):c.8071C>T (p.Arg2691Cys) rs531980488
NM_000051.4(ATM):c.8560C>T (p.Arg2854Cys) rs201958469
NM_000051.4(ATM):c.8948C>T (p.Thr2983Ile)
NM_000051.4(ATM):c.9023G>A (p.Arg3008His) rs587781894
NM_000051.4(ATM):c.9091C>T (p.Gln3031Ter)
NM_001330368.2(C11orf65):c.640+20516del rs1591387383
NM_001330368.2(C11orf65):c.641-22822_641-22814del rs587776547

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