ClinVar Miner

List of variants in gene CNGB1 reported as benign for not provided

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Gene type:
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Total variants: 84
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HGVS dbSNP gnomAD frequency
NM_001297.5(CNGB1):c.875-39C>T rs152143 0.98924
NM_001297.5(CNGB1):c.2635-10C>T rs437920 0.77649
NM_001297.5(CNGB1):c.217+46G>A rs3859043 0.71272
NM_001297.5(CNGB1):c.838-36G>A rs503686 0.66487
NM_001297.5(CNGB1):c.1801+23T>C rs166000 0.63352
NM_001297.5(CNGB1):c.2218-12C>T rs483053 0.49394
NM_001297.5(CNGB1):c.1122-15C>T rs2303778 0.46316
NM_001297.5(CNGB1):c.3462+7T>C rs11076207 0.37846
NM_001297.5(CNGB1):c.327C>T (p.Gly109=) rs17821448 0.36916
NM_001297.5(CNGB1):c.2193C>T (p.Asn731=) rs376270 0.31387
NM_001297.5(CNGB1):c.1958-14A>C rs3991715 0.30656
NM_001297.5(CNGB1):c.534+20G>A rs2288485 0.17092
NM_001297.5(CNGB1):c.2233C>A (p.Leu745Ile) rs10459809 0.14066
NM_001297.5(CNGB1):c.1644T>C (p.Asp548=) rs2161703 0.12201
NM_001297.5(CNGB1):c.*310T>C rs57309302 0.11688
NM_001297.5(CNGB1):c.*33A>G rs13338071 0.11360
NM_001297.5(CNGB1):c.2732A>G (p.Lys911Arg) rs2303785 0.09003
NM_001297.5(CNGB1):c.1950G>C (p.Pro650=) rs35424571 0.06391
NM_001297.5(CNGB1):c.1604T>C (p.Val535Ala) rs12927214 0.05861
NM_001297.5(CNGB1):c.2882C>T (p.Ala961Val) rs112002818 0.04422
NM_001297.5(CNGB1):c.440T>G (p.Leu147Arg) rs61997173 0.03447
NM_001297.5(CNGB1):c.534+7C>G rs16959600 0.03025
NM_001297.5(CNGB1):c.1473G>A (p.Pro491=) rs9925973 0.03012
NM_001297.5(CNGB1):c.2517T>C (p.Ala839=) rs17821412 0.02990
NM_001297.5(CNGB1):c.453C>T (p.Asp151=) rs16959602 0.02909
NM_001297.5(CNGB1):c.2892+6C>T rs16942441 0.02754
NM_001297.5(CNGB1):c.3556C>T (p.Pro1186Ser) rs7190372 0.02335
NM_001297.5(CNGB1):c.218-18T>C rs115569700 0.02150
NM_001297.5(CNGB1):c.2854G>A (p.Val952Met) rs79889567 0.02046
NM_001297.5(CNGB1):c.105G>A (p.Ala35=) rs61997250 0.01885
NM_001297.5(CNGB1):c.3378C>T (p.Gly1126=) rs11867123 0.01433
NM_001297.5(CNGB1):c.712G>A (p.Gly238Ser) rs61745888 0.01420
NM_001297.5(CNGB1):c.606A>G (p.Glu202=) rs76788887 0.01379
NM_001297.5(CNGB1):c.1643+13del rs3217335 0.01152
NM_001297.5(CNGB1):c.2481C>T (p.Gly827=) rs77399988 0.01073
NM_001297.5(CNGB1):c.3527C>T (p.Pro1176Leu) rs73562944 0.00971
NM_001297.5(CNGB1):c.1373-11C>A rs2303782 0.00856
NM_001297.5(CNGB1):c.1382C>T (p.Thr461Met) rs147593839 0.00762
NM_001297.5(CNGB1):c.2700G>A (p.Thr900=) rs72782250 0.00722
NM_001297.5(CNGB1):c.1500C>T (p.Thr500=) rs75406397 0.00513
NM_001297.5(CNGB1):c.1122-18C>T rs79540781 0.00494
NM_001297.5(CNGB1):c.123G>A (p.Pro41=) rs41482547 0.00487
NM_001297.5(CNGB1):c.634A>T (p.Thr212Ser) rs192628905 0.00486
NM_001297.5(CNGB1):c.1479G>A (p.Pro493=) rs1052029 0.00308
NM_001297.5(CNGB1):c.1626C>T (p.Thr542=) rs148735841 0.00304
NM_001297.5(CNGB1):c.159+14C>T rs199591689 0.00255
NM_001297.5(CNGB1):c.3147C>T (p.His1049=) rs200581517 0.00255
NM_001297.5(CNGB1):c.1580C>T (p.Ala527Val) rs78292723 0.00242
NM_001297.5(CNGB1):c.761+15A>G rs187864931 0.00227
NM_001297.5(CNGB1):c.376G>C (p.Ala126Pro) rs200332871 0.00219
NM_001297.5(CNGB1):c.3340G>A (p.Ala1114Thr) rs200242407 0.00213
NM_001297.5(CNGB1):c.2475C>T (p.Tyr825=) rs200934249 0.00180
NM_001297.5(CNGB1):c.2514T>C (p.Phe838=) rs370767664 0.00178
NM_001297.5(CNGB1):c.1204G>A (p.Asp402Asn) rs140907154 0.00175
NM_001297.5(CNGB1):c.2492+19C>G rs184343851 0.00096
NM_001297.5(CNGB1):c.3135C>T (p.Asn1045=) rs539304668 0.00075
NM_001297.5(CNGB1):c.2526C>T (p.Thr842=) rs185729258 0.00074
NM_001297.5(CNGB1):c.3584C>G (p.Ser1195Cys) rs201186180 0.00066
NM_001297.5(CNGB1):c.595C>T (p.Arg199Cys) rs199583058 0.00054
NM_001297.5(CNGB1):c.3717G>T (p.Ser1239=) rs202083169 0.00052
NM_001297.5(CNGB1):c.1631C>T (p.Pro544Leu) rs145234666 0.00044
NM_001297.5(CNGB1):c.2850C>T (p.Ile950=) rs563734833 0.00038
NM_001297.5(CNGB1):c.933G>A (p.Pro311=) rs557276296 0.00032
NM_001297.5(CNGB1):c.1435C>A (p.Leu479Ile) rs2303783 0.00031
NM_001297.5(CNGB1):c.412+8C>A rs185727761 0.00030
NM_001297.5(CNGB1):c.139G>A (p.Glu47Lys) rs78149232 0.00023
NM_001297.5(CNGB1):c.458+7C>T rs368819628 0.00016
NM_001297.5(CNGB1):c.2976+8G>C rs374813501 0.00014
NM_001297.5(CNGB1):c.3366G>A (p.Lys1122=) rs751822516 0.00011
NM_001297.5(CNGB1):c.3309G>A (p.Ala1103=) rs201319323 0.00004
NM_001297.5(CNGB1):c.3560G>A (p.Arg1187Gln) rs543712958 0.00004
NM_001297.5(CNGB1):c.90G>A (p.Glu30=) rs375219355 0.00002
NM_001297.5(CNGB1):c.1089GGA[6] (p.Glu371dup) rs141566950
NM_001297.5(CNGB1):c.1275C>G (p.Ala425=) rs376016716
NM_001297.5(CNGB1):c.1643+39C>G rs247065
NM_001297.5(CNGB1):c.1957+11G>A rs190910346
NM_001297.5(CNGB1):c.2217+9C>T rs368099688
NM_001297.5(CNGB1):c.2369+13del rs1960769381
NM_001297.5(CNGB1):c.257G>A (p.Arg86Gln) rs8055343
NM_001297.5(CNGB1):c.2664C>A (p.Ala888=) rs413562
NM_001297.5(CNGB1):c.2664C>G (p.Ala888=) rs413562
NM_001297.5(CNGB1):c.2853C>A (p.Asp951Glu) rs7190978
NM_001297.5(CNGB1):c.2881G>T (p.Ala961Ser) rs16942445
NM_001297.5(CNGB1):c.299G>A (p.Arg100His) rs13336595

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