ClinVar Miner

List of variants in gene combination FBXO11, MSH6 reported as likely benign for not provided

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Gene type:
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Total variants: 90
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HGVS dbSNP gnomAD frequency
NM_000179.3(MSH6):c.*85T>A rs2020906 0.00645
NM_001190274.2(FBXO11):c.2436G>A (p.Val812=) rs148676301 0.00029
NM_001190274.2(FBXO11):c.2654+12A>G rs370468658 0.00009
NM_001190274.2(FBXO11):c.2433T>C (p.Asn811=) rs893463495 0.00006
NM_001190274.2(FBXO11):c.2654+13C>G rs375824193 0.00005
NM_001190274.2(FBXO11):c.2447-11_2447-8del rs368651175 0.00004
NM_001190274.2(FBXO11):c.2458A>G (p.Met820Val) rs747122948 0.00004
NM_001190274.2(FBXO11):c.2718A>C (p.Thr906=) rs533101051 0.00004
NM_001190274.2(FBXO11):c.2590A>G (p.Ile864Val) rs373629400 0.00002
NM_001190274.2(FBXO11):c.2736A>G (p.Leu912=) rs377413299 0.00002
NM_001190274.2(FBXO11):c.2358C>T (p.His786=) rs757286262 0.00001
NM_001190274.2(FBXO11):c.2555+13T>C rs928681621 0.00001
NM_001190274.2(FBXO11):c.2555+7T>A rs370587312 0.00001
NM_001190274.2(FBXO11):c.2655-13del rs1194699134 0.00001
NM_001190274.2(FBXO11):c.2655-9T>C rs767671883 0.00001
NM_001190274.2(FBXO11):c.2781C>T (p.Asn927=) rs756515981 0.00001
NC_000002.11:g.(?_48010373)_(48066928_?)dup
NM_000179.3(MSH6):c.4068_4071dup (p.Lys1358delinsAspTer) rs55740729
NM_001190274.2(FBXO11):c.2339-4T>G rs113217589
NM_001190274.2(FBXO11):c.2339-8_2339-4del
NM_001190274.2(FBXO11):c.2364T>A (p.Thr788=)
NM_001190274.2(FBXO11):c.2373A>G (p.Leu791=)
NM_001190274.2(FBXO11):c.2385G>C (p.Gln795His)
NM_001190274.2(FBXO11):c.2400G>A (p.Arg800=)
NM_001190274.2(FBXO11):c.2409C>T (p.Gly803=)
NM_001190274.2(FBXO11):c.2415T>C (p.Phe805=) rs2104625984
NM_001190274.2(FBXO11):c.2446+11G>T
NM_001190274.2(FBXO11):c.2446+14T>C rs2104625718
NM_001190274.2(FBXO11):c.2446+15G>C
NM_001190274.2(FBXO11):c.2446+17T>G
NM_001190274.2(FBXO11):c.2446+18A>G
NM_001190274.2(FBXO11):c.2447-10T>C
NM_001190274.2(FBXO11):c.2447-12C>A
NM_001190274.2(FBXO11):c.2447-12C>G rs2104622586
NM_001190274.2(FBXO11):c.2447-12_2447-11del
NM_001190274.2(FBXO11):c.2447-12_2447-8del rs764710246
NM_001190274.2(FBXO11):c.2447-12_2447-9del rs752742195
NM_001190274.2(FBXO11):c.2447-13dup rs764057797
NM_001190274.2(FBXO11):c.2447-16C>T
NM_001190274.2(FBXO11):c.2447-16_2447-14del
NM_001190274.2(FBXO11):c.2447-18T>C
NM_001190274.2(FBXO11):c.2447-19_2447-16del
NM_001190274.2(FBXO11):c.2447-19_2447-17del rs756698768
NM_001190274.2(FBXO11):c.2447-20T>C
NM_001190274.2(FBXO11):c.2447-22_2447-19del
NM_001190274.2(FBXO11):c.2447-6T>C
NM_001190274.2(FBXO11):c.2447-8T>A rs769854268
NM_001190274.2(FBXO11):c.2447-8T>C
NM_001190274.2(FBXO11):c.2447-9_2447-5del
NM_001190274.2(FBXO11):c.2477T>C (p.Ile826Thr)
NM_001190274.2(FBXO11):c.2502A>G (p.Gln834=)
NM_001190274.2(FBXO11):c.2526T>C (p.Tyr842=)
NM_001190274.2(FBXO11):c.2555+12A>G
NM_001190274.2(FBXO11):c.2555+14dup
NM_001190274.2(FBXO11):c.2555+15T>C
NM_001190274.2(FBXO11):c.2555+16_2555+19del
NM_001190274.2(FBXO11):c.2555+18_2555+19del
NM_001190274.2(FBXO11):c.2555+19T>C rs2104621277
NM_001190274.2(FBXO11):c.2555+19dup
NM_001190274.2(FBXO11):c.2556-11T>C
NM_001190274.2(FBXO11):c.2556-14C>T rs1370502206
NM_001190274.2(FBXO11):c.2556-19T>G rs1460227977
NM_001190274.2(FBXO11):c.2556-6T>C
NM_001190274.2(FBXO11):c.2556-7T>G
NM_001190274.2(FBXO11):c.2574C>G (p.Thr858=)
NM_001190274.2(FBXO11):c.2574C>T (p.Thr858=)
NM_001190274.2(FBXO11):c.2598G>A (p.Val866=)
NM_001190274.2(FBXO11):c.2619T>C (p.His873=)
NM_001190274.2(FBXO11):c.2628T>C (p.His876=)
NM_001190274.2(FBXO11):c.2634A>T (p.Val878=)
NM_001190274.2(FBXO11):c.2654+10A>G
NM_001190274.2(FBXO11):c.2654+16G>A rs1476099824
NM_001190274.2(FBXO11):c.2654+16dup
NM_001190274.2(FBXO11):c.2654+19T>C
NM_001190274.2(FBXO11):c.2654+20_2654+24del
NM_001190274.2(FBXO11):c.2654+8G>A
NM_001190274.2(FBXO11):c.2654+8G>T rs2104612750
NM_001190274.2(FBXO11):c.2655-16T>C
NM_001190274.2(FBXO11):c.2655-17G>C
NM_001190274.2(FBXO11):c.2655-20T>G
NM_001190274.2(FBXO11):c.2655-6C>T
NM_001190274.2(FBXO11):c.2655-9T>G
NM_001190274.2(FBXO11):c.2670T>C (p.Cys890=)
NM_001190274.2(FBXO11):c.2673T>C (p.Gly891=)
NM_001190274.2(FBXO11):c.2675C>T (p.Ala892Val) rs1670358755
NM_001190274.2(FBXO11):c.2691T>C (p.Asn897=) rs2104611324
NM_001190274.2(FBXO11):c.2728G>A (p.Asp910Asn) rs2104610803
NM_001190274.2(FBXO11):c.2734C>T (p.Leu912=)
NM_001190274.2(FBXO11):c.2748T>C (p.Ala916=)
NM_001190274.2(FBXO11):c.2763T>C (p.Ser921=)

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