ClinVar Miner

List of variants in gene combination ARID1B, LOC115308161 reported by Genetic Services Laboratory, University of Chicago

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Total variants: 16
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HGVS dbSNP gnomAD frequency
NM_001374828.1(ARID1B):c.612A>G (p.Gln204=) rs78253128 0.00509
NM_001374828.1(ARID1B):c.347C>T (p.Ala116Val) rs1325414473 0.00001
NM_001374828.1(ARID1B):c.352TCC[6] (p.Ser124del) rs770512547
NM_001374828.1(ARID1B):c.352TCC[8] (p.Ser124dup) rs770512547
NM_001374828.1(ARID1B):c.369C>T (p.Ser123=) rs1281627380
NM_001374828.1(ARID1B):c.527A>T (p.His176Leu) rs587779741
NM_001374828.1(ARID1B):c.537_560del (p.His181_Ala188del) rs1554247278
NM_001374828.1(ARID1B):c.591GCA[8] (p.Gln214dup) rs587779743
NM_001374828.1(ARID1B):c.591GCA[9] (p.Gln213_Gln214dup) rs587779743
NM_001374828.1(ARID1B):c.594GCAGCAGCAGCAGCAGCAACAGCA[3] (p.Gln207_Gln214dup) rs770869529
NM_001374828.1(ARID1B):c.612_620del (p.Gln212_Gln214del) rs797045274
NM_001374828.1(ARID1B):c.612_623del (p.Gln211_Gln214del) rs797045275
NM_001374828.1(ARID1B):c.612_632del (p.Gln208_Gln214del) rs762617219
NM_001374828.1(ARID1B):c.615GCA[6] (p.Gln214del) rs587779744
NM_001374828.1(ARID1B):c.615GCA[8] (p.Gln214dup) rs587779744
NM_001374828.1(ARID1B):c.615GCA[9] (p.Gln213_Gln214dup) rs587779744

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