ClinVar Miner

List of variants in gene ARID1B reported as likely pathogenic for not provided

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Gene type:
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Total variants: 37
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HGVS dbSNP gnomAD frequency
NM_001374828.1(ARID1B):c.3236-1G>A rs752642190 0.00001
GRCh37/hg19 6q25.3(chr6:156234522-157126587)x1
GRCh37/hg19 6q25.3(chr6:157201571-157340945)x1
GRCh37/hg19 6q25.3(chr6:157402040-157432660)x1
GRCh37/hg19 6q25.3(chr6:157431664-157482864)x1
NC_000006.11:g.(?_157488154)_(157505589_?)dup
NM_001374828.1(ARID1B):c.1719G>A (p.Trp573Ter) rs1779020146
NM_001374828.1(ARID1B):c.1781del (p.Gly594fs) rs1779031164
NM_001374828.1(ARID1B):c.2170C>T (p.Gln724Ter) rs1554270809
NM_001374828.1(ARID1B):c.2248-2A>G rs2128462015
NM_001374828.1(ARID1B):c.2581+5G>A rs1554298239
NM_001374828.1(ARID1B):c.2581G>A (p.Gly861Ser) rs1057518045
NM_001374828.1(ARID1B):c.2762-1G>C
NM_001374828.1(ARID1B):c.2762-2A>C rs770350755
NM_001374828.1(ARID1B):c.3089+2T>C rs1057518318
NM_001374828.1(ARID1B):c.3258G>T (p.Met1086Ile) rs1057518059
NM_001374828.1(ARID1B):c.3345G>A (p.Lys1115=) rs1583451360
NM_001374828.1(ARID1B):c.3665A>T (p.Asp1222Val) rs1554231259
NM_001374828.1(ARID1B):c.3704G>A (p.Gly1235Asp) rs864309615
NM_001374828.1(ARID1B):c.3715-2A>G
NM_001374828.1(ARID1B):c.4192delinsCATGAGCCCA (p.Tyr1398delinsHisGluProAsn) rs1554233151
NM_001374828.1(ARID1B):c.4656G>A (p.Arg1552=)
NM_001374828.1(ARID1B):c.4712del (p.Met1571fs) rs1794059063
NM_001374828.1(ARID1B):c.5264-2A>C rs1794274425
NM_001374828.1(ARID1B):c.5763_5766del (p.Phe1921fs) rs1554237269
NM_001374828.1(ARID1B):c.5773C>T (p.Arg1925Ter) rs797045282
NM_001374828.1(ARID1B):c.5831_5835del (p.Leu1944fs) rs1131691508
NM_001374828.1(ARID1B):c.5968dup (p.Glu1990fs) rs1554237473
NM_001374828.1(ARID1B):c.6145C>T (p.Arg2049Ter) rs1554237658
NM_001374828.1(ARID1B):c.6319G>T (p.Glu2107Ter) rs786205584
NM_001374828.1(ARID1B):c.6404G>A (p.Trp2135Ter) rs1554237845
NM_001374828.1(ARID1B):c.6461T>C (p.Ile2154Thr) rs2128397101
NM_001374828.1(ARID1B):c.6464C>T (p.Ser2155Phe) rs886039594
NM_001374828.1(ARID1B):c.6493G>A (p.Glu2165Lys) rs1064794799
NM_001374828.1(ARID1B):c.6716_6719del (p.Val2239fs) rs1794555916
NM_001374828.1(ARID1B):c.6726_6730dup (p.Asp2244fs) rs2128398237
NM_001374828.1(ARID1B):c.6775T>C (p.Ser2259Pro) rs1057521854

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