ClinVar Miner

List of variants in gene TAB2 reported as likely benign for not provided

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Gene type:
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Total variants: 54
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HGVS dbSNP gnomAD frequency
NM_001292034.3(TAB2):c.282A>G (p.Gly94=) rs13215304 0.02185
NM_001292034.3(TAB2):c.1859-126G>C rs34590971 0.01268
NM_001292034.3(TAB2):c.1859-140A>G rs35800835 0.00952
NM_001292034.3(TAB2):c.-89-238G>A rs35375829 0.00892
NM_001292034.3(TAB2):c.1603+292T>C rs140391735 0.00812
NM_001292034.3(TAB2):c.*286A>C rs34532338 0.00728
NM_001292034.3(TAB2):c.1940-253G>A rs187457066 0.00657
NM_001292034.3(TAB2):c.1604-190C>T rs36103023 0.00500
NM_001292034.3(TAB2):c.438T>C (p.Ser146=) rs150852637 0.00063
NM_001292034.3(TAB2):c.597T>G (p.Gly199=) rs115168915 0.00055
NM_001292034.3(TAB2):c.472C>T (p.His158Tyr) rs139897844 0.00046
NM_001292034.3(TAB2):c.156A>G (p.Arg52=) rs143213478 0.00012
NM_001292034.3(TAB2):c.311C>T (p.Thr104Met) rs559771770 0.00009
NM_001292034.3(TAB2):c.507A>G (p.Gln169=) rs962520265 0.00006
NM_001292034.3(TAB2):c.1878C>T (p.Ser626=) rs376467260 0.00005
NM_001292034.3(TAB2):c.165T>C (p.Tyr55=) rs775402300 0.00004
NM_001292034.3(TAB2):c.102+12A>G rs370126366 0.00002
NM_001292034.3(TAB2):c.588C>T (p.His196=) rs758431534 0.00001
NM_001292034.3(TAB2):c.102+10del
NM_001292034.3(TAB2):c.102+14G>A
NM_001292034.3(TAB2):c.102+17T>C
NM_001292034.3(TAB2):c.102+17T>G rs770691939
NM_001292034.3(TAB2):c.103-12T>C
NM_001292034.3(TAB2):c.103-4A>G
NM_001292034.3(TAB2):c.138C>T (p.Leu46=)
NM_001292034.3(TAB2):c.1604-148dup rs375953182
NM_001292034.3(TAB2):c.1604-14A>G
NM_001292034.3(TAB2):c.1604-169_1604-168del rs201262923
NM_001292034.3(TAB2):c.1604-4G>A
NM_001292034.3(TAB2):c.1662A>G (p.Gln554=)
NM_001292034.3(TAB2):c.1668A>G (p.Lys556=)
NM_001292034.3(TAB2):c.1779G>A (p.Gln593=)
NM_001292034.3(TAB2):c.1858+11G>A
NM_001292034.3(TAB2):c.1858+19G>A
NM_001292034.3(TAB2):c.1858+20T>C
NM_001292034.3(TAB2):c.1858+9C>A
NM_001292034.3(TAB2):c.1859-12T>C
NM_001292034.3(TAB2):c.1859-92C>A rs36071026
NM_001292034.3(TAB2):c.1860A>G (p.Gly620=)
NM_001292034.3(TAB2):c.18C>T (p.His6=)
NM_001292034.3(TAB2):c.1905T>C (p.Ile635=)
NM_001292034.3(TAB2):c.1929A>G (p.Pro643=)
NM_001292034.3(TAB2):c.1939+19T>C
NM_001292034.3(TAB2):c.1940-11C>T rs2114979212
NM_001292034.3(TAB2):c.1940-16T>G
NM_001292034.3(TAB2):c.2013C>T (p.Thr671=)
NM_001292034.3(TAB2):c.207T>C (p.Ser69=)
NM_001292034.3(TAB2):c.297A>G (p.Gly99=)
NM_001292034.3(TAB2):c.324T>C (p.Ser108=) rs1200884981
NM_001292034.3(TAB2):c.333A>G (p.Gln111=)
NM_001292034.3(TAB2):c.351C>T (p.Ser117=) rs1781473281
NM_001292034.3(TAB2):c.450T>C (p.Asn150=)
NM_001292034.3(TAB2):c.459A>G (p.Pro153=)
NM_001292034.3(TAB2):c.474C>T (p.His158=)

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