List of variants in gene combination ATM, C11orf65 reported as uncertain significance by Athena Diagnostics Inc

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 50

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HGVS	dbSNP	gnomAD frequency
NM_000051.4(ATM):c.7740A>C (p.Arg2580Ser)	rs199915459	0.00031
NM_000051.4(ATM):c.6537T>G (p.Ile2179Met)	rs146243469	0.00022
NM_000051.4(ATM):c.5821G>C (p.Val1941Leu)	rs147187700	0.00019
NM_000051.4(ATM):c.8734A>G (p.Arg2912Gly)	rs376676328	0.00019
NM_000051.4(ATM):c.9086G>A (p.Gly3029Asp)	rs201199629	0.00016
NM_000051.4(ATM):c.8156G>A (p.Arg2719His)	rs55982963	0.00015
NM_000051.4(ATM):c.6194T>C (p.Ile2065Thr)	rs372838622	0.00014
NM_000051.4(ATM):c.7618G>A (p.Val2540Ile)	rs35203200	0.00014
NM_000051.4(ATM):c.8560C>T (p.Arg2854Cys)	rs201958469	0.00013
NM_000051.4(ATM):c.7494T>C (p.Ser2498=)	rs34393781	0.00010
NM_000051.4(ATM):c.6820G>A (p.Ala2274Thr)	rs567060474	0.00009
NM_000051.4(ATM):c.8495G>A (p.Arg2832His)	rs529296539	0.00006
NM_000051.4(ATM):c.9031A>G (p.Met3011Val)	rs372795527	0.00005
NM_000051.4(ATM):c.6179G>C (p.Arg2060Pro)	rs376521407	0.00004
NM_000051.4(ATM):c.7592T>C (p.Met2531Thr)	rs587781365	0.00004
NM_000051.4(ATM):c.8558C>T (p.Thr2853Met)	rs141534716	0.00004
NM_000051.4(ATM):c.6814G>A (p.Glu2272Lys)	rs886039471	0.00002
NM_000051.4(ATM):c.7358G>A (p.Arg2453His)	rs587781361	0.00002
NM_000051.4(ATM):c.8405A>G (p.Gln2802Arg)	rs730881324	0.00002
NM_000051.4(ATM):c.8520G>C (p.Leu2840Phe)	rs752652869	0.00002
NM_000051.4(ATM):c.5892G>C (p.Lys1964Asn)	rs786202728	0.00001
NM_000051.4(ATM):c.6154G>A (p.Glu2052Lys)	rs202206540	0.00001
NM_000051.4(ATM):c.6536T>C (p.Ile2179Thr)	rs878853532	0.00001
NM_000051.4(ATM):c.6807G>A (p.Gln2269=)	rs587780638	0.00001
NM_000051.4(ATM):c.6975+5G>T	rs575354684	0.00001
NM_000051.4(ATM):c.7382G>A (p.Arg2461His)	rs768461085	0.00001
NM_000051.4(ATM):c.7499T>C (p.Val2500Ala)	rs779810877	0.00001
NM_000051.4(ATM):c.7502A>G (p.Asn2501Ser)	rs531617441	0.00001
NM_000051.4(ATM):c.8314G>A (p.Gly2772Arg)	rs1064794239	0.00001
NM_000051.4(ATM):c.8617G>A (p.Val2873Ile)	rs730881327	0.00001
NM_000051.4(ATM):c.9041A>G (p.Gln3014Arg)	rs1064793579	0.00001
NM_000051.4(ATM):c.*5del
NM_000051.4(ATM):c.5822T>G (p.Val1941Gly)	rs876660334
NM_000051.4(ATM):c.5887G>A (p.Asp1963Asn)	rs864622148
NM_000051.4(ATM):c.6248G>C (p.Gly2083Ala)	rs1060501559
NM_000051.4(ATM):c.6583C>T (p.His2195Tyr)	rs780946471
NM_000051.4(ATM):c.6859G>A (p.Gly2287Arg)	rs1181779478
NM_000051.4(ATM):c.6878T>C (p.Leu2293Pro)	rs1450429233
NM_000051.4(ATM):c.6975+4T>G	rs876660240
NM_000051.4(ATM):c.6975G>A (p.Ala2325=)	rs556778314
NM_000051.4(ATM):c.6975G>C (p.Ala2325=)	rs556778314
NM_000051.4(ATM):c.7235A>G (p.Asn2412Ser)	rs786203311
NM_000051.4(ATM):c.7339T>G (p.Leu2447Val)	rs1591159997
NM_000051.4(ATM):c.7375C>G (p.Arg2459Gly)	rs730881383
NM_000051.4(ATM):c.8187A>T (p.Gln2729His)	rs587781946
NM_000051.4(ATM):c.8311A>G (p.Thr2771Ala)	rs876660587
NM_000051.4(ATM):c.8486C>A (p.Pro2829Gln)	rs938431501
NM_000051.4(ATM):c.8495G>T (p.Arg2832Leu)	rs529296539
NM_000051.4(ATM):c.8536T>C (p.Phe2846Leu)	rs1591265229
NM_000051.4(ATM):c.8917A>G (p.Arg2973Gly)	rs1555151352

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