List of variants in gene combination ATM, C11orf65 reported as not provided

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: 53

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HGVS	dbSNP	gnomAD frequency
NM_000051.4(ATM):c.6995T>C (p.Leu2332Pro)	rs4988111	0.00660
NM_000051.4(ATM):c.6235G>A (p.Val2079Ile)	rs1800060	0.00649
NM_000051.4(ATM):c.6088A>G (p.Ile2030Val)	rs145847315	0.00517
NM_000051.4(ATM):c.6437G>C (p.Ser2146Thr)	rs56815840	0.00424
NM_000051.4(ATM):c.6067G>A (p.Gly2023Arg)	rs11212587	0.00124
NM_000051.4(ATM):c.6919C>T (p.Leu2307Phe)	rs56009889	0.00035
NM_000051.4(ATM):c.7174C>T (p.Arg2392Trp)	rs149827260	0.00030
NM_000051.4(ATM):c.7004C>T (p.Thr2335Ile)	rs3092831	0.00029
NM_000051.4(ATM):c.7516A>G (p.Arg2506Gly)	rs200441272	0.00019
NM_000051.4(ATM):c.8734A>G (p.Arg2912Gly)	rs376676328	0.00019
NM_000051.4(ATM):c.7187C>G (p.Thr2396Ser)	rs370559102	0.00017
NM_000051.4(ATM):c.7381C>T (p.Arg2461Cys)	rs201314561	0.00017
NM_000051.4(ATM):c.9086G>A (p.Gly3029Asp)	rs201199629	0.00016
NM_000051.4(ATM):c.8560C>T (p.Arg2854Cys)	rs201958469	0.00013
NM_000051.4(ATM):c.6343G>A (p.Val2115Ile)	rs587780634	0.00011
NM_000051.4(ATM):c.7919C>T (p.Thr2640Ile)	rs4988125	0.00011
NM_000051.4(ATM):c.8071C>T (p.Arg2691Cys)	rs531980488	0.00011
NM_000051.4(ATM):c.7988T>C (p.Val2663Ala)	rs377648506	0.00010
NM_000051.4(ATM):c.6475T>G (p.Cys2159Gly)	rs150408832	0.00009
NM_000051.4(ATM):c.7757A>G (p.Asn2586Ser)	rs587778079	0.00009
NM_000051.4(ATM):c.7271T>G (p.Val2424Gly)	rs28904921	0.00006
NM_000051.4(ATM):c.8495G>A (p.Arg2832His)	rs529296539	0.00006
NM_000051.4(ATM):c.5763-1050A>G	rs774925473	0.00004
NM_000051.4(ATM):c.5932G>T (p.Glu1978Ter)	rs587779852	0.00004
NM_000051.4(ATM):c.8147T>C (p.Val2716Ala)	rs587782652	0.00004
NM_000051.4(ATM):c.8968G>A (p.Glu2990Lys)	rs1800558	0.00004
NM_000051.4(ATM):c.8120C>G (p.Ser2707Cys)	rs748016261	0.00002
NM_000051.4(ATM):c.8129A>G (p.Lys2710Arg)	rs587782001	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.6679C>T (p.Arg2227Cys)	rs564652222	0.00001
NM_000051.4(ATM):c.7463G>A (p.Cys2488Tyr)	rs774281788	0.00001
NM_000051.4(ATM):c.7630-2A>C	rs587779866	0.00001
NM_000051.4(ATM):c.8393C>A (p.Ala2798Asp)	rs772992098	0.00001
NM_000051.4(ATM):c.8494C>T (p.Arg2832Cys)	rs587779872	0.00001
NM_000051.4(ATM):c.8545C>T (p.Arg2849Ter)	rs587778080	0.00001
NM_000051.4(ATM):c.8978G>A (p.Arg2993Gln)	rs587778081	0.00001
NM_000051.4(ATM):c.8983C>A (p.Leu2995Ile)	rs142322668	0.00001
NM_000051.3(ATM):c.5945A>T (p.Gln1982Leu)	rs543980602
NM_000051.4(ATM):c.5784dup (p.Asn1929Ter)	rs1131691254
NM_000051.4(ATM):c.5948= (p.Ser1983=)	rs659243
NM_000051.4(ATM):c.6178C>T (p.Arg2060Cys)	rs587778078
NM_000051.4(ATM):c.6200C>A (p.Ala2067Asp)	rs397514577
NM_000051.4(ATM):c.6916_6917del (p.Leu2307fs)	rs878853535
NM_000051.4(ATM):c.7875_7876delinsGC (p.Asp2625_Ala2626delinsGluPro)	rs267606668
NM_000051.4(ATM):c.7886_7890del (p.Ile2629fs)	rs1450394308
NM_000051.4(ATM):c.8036_8051del (p.Asn2679fs)	rs587780640
NM_000051.4(ATM):c.8264A>C (p.Tyr2755Ser)	rs1591199410
NM_000051.4(ATM):c.8269-10_8269-9del	rs587780641
NM_000051.4(ATM):c.8552C>T (p.Ala2851Val)	rs876659701
NM_000051.4(ATM):c.8565T>G (p.Ser2855Arg)	rs780905851
NM_000051.4(ATM):c.8623A>C (p.Asn2875His)	rs1057519869
NM_000051.4(ATM):c.8879G>A (p.Trp2960Ter)	rs1131691149

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