List of variants in gene combination ATM, C11orf65 reported as uncertain significance 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: 32

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HGVS	dbSNP	gnomAD frequency
NM_000051.4(ATM):c.7313C>T (p.Thr2438Ile)	rs147604227	0.00056
NM_000051.4(ATM):c.7174C>T (p.Arg2392Trp)	rs149827260	0.00030
NM_000051.4(ATM):c.5975A>C (p.Lys1992Thr)	rs150757822	0.00025
NM_000051.4(ATM):c.7919C>T (p.Thr2640Ile)	rs4988125	0.00011
NM_000051.4(ATM):c.6315G>C (p.Arg2105Ser)	rs587780632	0.00006
NM_000051.4(ATM):c.8921C>T (p.Pro2974Leu)	rs139379666	0.00006
NM_000051.4(ATM):c.6101G>A (p.Arg2034Gln)	rs3218670	0.00004
NM_000051.4(ATM):c.8428A>C (p.Lys2810Gln)	rs730881325	0.00004
NM_000051.4(ATM):c.8558C>T (p.Thr2853Met)	rs141534716	0.00004
NM_000051.4(ATM):c.8968G>A (p.Glu2990Lys)	rs1800558	0.00004
NM_000051.4(ATM):c.6814G>A (p.Glu2272Lys)	rs886039471	0.00002
NM_000051.4(ATM):c.7808A>G (p.Asn2603Ser)	rs150355232	0.00002
NM_000051.4(ATM):c.6154G>A (p.Glu2052Lys)	rs202206540	0.00001
NM_000051.4(ATM):c.7399G>A (p.Val2467Ile)	rs769722643	0.00001
NM_000051.4(ATM):c.7996A>G (p.Thr2666Ala)	rs745775382	0.00001
NM_000051.4(ATM):c.8000T>C (p.Met2667Thr)	rs1060501566	0.00001
NM_000051.4(ATM):c.8047A>G (p.Ile2683Val)	rs587781344	0.00001
NM_000051.4(ATM):c.8268+13A>T	rs1400036072	0.00001
NM_000051.4(ATM):c.8965C>G (p.Gln2989Glu)	rs147695170	0.00001
NM_000051.4(ATM):c.5918+3A>G	rs1555110595
NM_000051.4(ATM):c.5961T>C (p.Ser1987=)	rs1060504265
NM_000051.4(ATM):c.6335G>A (p.Cys2112Tyr)	rs1591790360
NM_000051.4(ATM):c.6608T>C (p.Ile2203Thr)	rs2085553784
NM_000051.4(ATM):c.6860G>A (p.Gly2287Glu)	rs1800061
NM_000051.4(ATM):c.6898T>G (p.Trp2300Gly)	rs1565520641
NM_000051.4(ATM):c.6975G>C (p.Ala2325=)	rs556778314
NM_000051.4(ATM):c.7164C>A (p.Leu2388=)	rs1239532344
NM_000051.4(ATM):c.7654C>A (p.His2552Asn)	rs786202174
NM_000051.4(ATM):c.7885A>G (p.Ile2629Val)	rs2136569929
NM_000051.4(ATM):c.8015A>C (p.Asp2672Ala)	rs763161651
NM_000051.4(ATM):c.8083G>T (p.Gly2695Cys)	rs1555127166
NM_000051.4(ATM):c.8850+12dup	rs1555143639

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