ClinVar Miner

List of variants studied for Common variable immunodeficiency

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Total variants: 16
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HGVS dbSNP
NM_003809.3(TNFSF12):c.177G>C (p.Glu59Asp)
NM_003809.3(TNFSF12):c.205_207dup (p.Ser69dup) rs753259588
NM_003809.3(TNFSF12):c.269G>A (p.Arg90Gln)
NM_003809.3(TNFSF12):c.338-9A>G rs114577645
NM_003809.3(TNFSF12):c.42G>A (p.Gly14=) rs1170763703
NM_003809.3(TNFSF12):c.43G>A (p.Glu15Lys) rs768061768
NM_003809.3(TNFSF12):c.443G>A (p.Arg148His)
NM_003809.3(TNFSF12):c.450C>T (p.Ile150=) rs147597489
NM_003809.3(TNFSF12):c.498+9del rs1356188583
NM_003809.3(TNFSF12):c.597G>A (p.Ala199=) rs143039184
NM_003809.3(TNFSF12):c.609C>T (p.Leu203=) rs140608168
NM_003809.3(TNFSF12):c.642G>T (p.Gly214=) rs4968189
NM_003809.3(TNFSF12):c.64G>C (p.Val22Leu)
NM_003809.3(TNFSF12):c.673C>T (p.Arg225Trp)
NM_003809.3(TNFSF12):c.679C>T (p.Arg227Cys) rs1414804824
NM_003809.3(TNFSF12):c.716T>C (p.Phe239Ser)

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