ClinVar Miner

List of variants in gene combination ATM, C11orf65 reported as uncertain significance by Illumina Clinical Services Laboratory,Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 46
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HGVS dbSNP
NM_000051.3(ATM):c.*1272C>G rs376572054
NM_000051.3(ATM):c.*1571C>T rs886047621
NM_000051.3(ATM):c.*1640C>T rs886047622
NM_000051.3(ATM):c.*1670G>A rs886047623
NM_000051.3(ATM):c.*1960del rs886047624
NM_000051.3(ATM):c.*2080C>T rs142456486
NM_000051.3(ATM):c.*2224C>T rs139245552
NM_000051.3(ATM):c.*222C>T rs760852487
NM_000051.3(ATM):c.*236C>T rs3092834
NM_000051.3(ATM):c.*2479G>A rs778439888
NM_000051.3(ATM):c.*2541_*2543del rs886047625
NM_000051.3(ATM):c.*2563C>T rs146547907
NM_000051.3(ATM):c.*2607T>C rs879796523
NM_000051.3(ATM):c.*2714dup rs532373195
NM_000051.3(ATM):c.*2779del rs886047627
NM_000051.3(ATM):c.*2865G>A rs568150944
NM_000051.3(ATM):c.*2866T>C rs191399133
NM_000051.3(ATM):c.*2935C>G rs886047628
NM_000051.3(ATM):c.*2957G>C rs770767475
NM_000051.3(ATM):c.*29C>G rs3218711
NM_000051.3(ATM):c.*3022C>G rs145076930
NM_000051.3(ATM):c.*3091G>A rs886047629
NM_000051.3(ATM):c.*3136A>G rs3092845
NM_000051.3(ATM):c.*3198T>G rs764033869
NM_000051.3(ATM):c.*3325A>G rs886047630
NM_000051.3(ATM):c.*3354T>G rs886047631
NM_000051.3(ATM):c.*44A>G rs55900855
NM_000051.3(ATM):c.*521del rs886047615
NM_000051.3(ATM):c.*540dup rs369583811
NM_000051.3(ATM):c.*541_*542del rs886047618
NM_000051.3(ATM):c.*541del rs886047619
NM_000051.3(ATM):c.*551T>C rs143531724
NM_000051.3(ATM):c.*684T>G rs3092837
NM_000051.3(ATM):c.*895dup rs200629108
NM_000051.3(ATM):c.6095+5A>G rs757328753
NM_000051.3(ATM):c.6203T>C (p.Leu2068Ser) rs1555114558
NM_000051.3(ATM):c.6382T>C (p.Leu2128=) rs753646931
NM_000051.3(ATM):c.6795C>T (p.Phe2265=) rs3218699
NM_000051.3(ATM):c.7223C>T (p.Ser2408Leu) rs730881315
NM_000051.3(ATM):c.7502A>G (p.Asn2501Ser) rs531617441
NM_000051.3(ATM):c.8246A>T (p.Lys2749Ile) rs779145081
NM_000051.3(ATM):c.8391T>C (p.Ser2797=) rs566485657
NM_000051.3(ATM):c.8481T>G (p.Phe2827Leu) rs886047614
NM_000051.3(ATM):c.8520G>C (p.Leu2840Phe) rs752652869
NM_000051.3(ATM):c.8851-3T>G rs748874219
NM_000051.3(ATM):c.8983C>A (p.Leu2995Ile) rs142322668

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