ClinVar Miner

List of variants in gene ARID1B reported as uncertain significance for not provided

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Total variants: 32
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HGVS dbSNP
NM_017519.2(ARID1B):c.1017_1019GGC[1] (p.Ala348_Ala350del) rs765410747
NM_017519.2(ARID1B):c.1022C>T (p.Ala341Val) rs1271802085
NM_017519.2(ARID1B):c.1032_1034GGC[5] (p.Ala350dup) rs764418312
NM_017519.2(ARID1B):c.1043_1045CAG[4] (p.Ala350dup) rs797045267
NM_017519.2(ARID1B):c.1044_1062dup (p.Gly355fs) rs943407609
NM_017519.2(ARID1B):c.1054_1056GGC[7] (p.Gly357dup) rs797045268
NM_017519.2(ARID1B):c.1370_1372CGG[5] (p.Ala460dup) rs757953295
NM_017519.2(ARID1B):c.1471_1472delinsAA (p.Ala491Lys) rs1562378975
NM_017519.2(ARID1B):c.2987-1G>A rs752642190
NM_017519.2(ARID1B):c.4097T>C (p.Met1366Thr) rs145012943
NM_017519.2(ARID1B):c.5910C>T (p.His1970=) rs142416998
NM_017519.2(ARID1B):c.652C>G (p.Pro218Ala) rs1044746171
NM_017519.2(ARID1B):c.679G>C (p.Val227Leu) rs777266582
NM_017519.2(ARID1B):c.679_680delinsCC (p.Val227Pro) rs1554247605
NM_017519.2(ARID1B):c.712G>T (p.Ala238Ser) rs1268089519
NM_017519.2(ARID1B):c.917C>G (p.Ala306Gly) rs1168284939
NM_017519.2(ARID1B):c.921_923CGG[3] (p.Gly315_Gly319del) rs587779747
NM_017519.2(ARID1B):c.921_923CGG[4] (p.Gly316_Gly319del) rs587779747
NM_017519.2(ARID1B):c.957_974dup (p.Ser320_Gly325dup)
NM_017519.2(ARID1B):c.958_981dup (p.Ser320_Gly327dup) rs1215031054
NM_017519.2(ARID1B):c.962_964GAG[4] (p.Gly325_Gly328del) rs747790383
NM_017519.2(ARID1B):c.986_994del (p.Ala329_Ala331del) rs1562377638
NM_020732.3(ARID1B):c.1685T>A (p.Ile562Asn) rs1057522610
NM_020732.3(ARID1B):c.2372-2A>C rs1057524160
NM_020732.3(ARID1B):c.2699C>T (p.Pro900Leu) rs1057521656
NM_020732.3(ARID1B):c.2960C>G (p.Ser987Cys) rs780818465
NM_020732.3(ARID1B):c.3007A>G (p.Met1003Val) rs764460073
NM_020732.3(ARID1B):c.3748A>C (p.Lys1250Gln) rs1057522635
NM_020732.3(ARID1B):c.4090G>A (p.Gly1364Ser) rs151115781
NM_020732.3(ARID1B):c.6519G>C (p.Gln2173His) rs1057522604
NM_020732.3(ARID1B):c.971G>C (p.Gly324Ala) rs1057522183
NM_020732.3(ARID1B):c.980G>C (p.Gly327Ala) rs1455234951

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