ClinVar Miner

List of variants in gene combination LOC130067574, TNFRSF13C reported as uncertain significance for immune system disorder

Included ClinVar conditions (908):
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Total variants: 59
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HGVS dbSNP gnomAD frequency
NM_052945.4(TNFRSF13C):c.191G>T (p.Gly64Val) rs547352394 0.00722
NM_052945.4(TNFRSF13C):c.60C>T (p.Val20=) rs373828157 0.00260
NM_052945.4(TNFRSF13C):c.317G>A (p.Arg106Gln) rs150374940 0.00202
NM_052945.4(TNFRSF13C):c.246C>T (p.Pro82=) rs779365266 0.00027
NM_052945.4(TNFRSF13C):c.213G>A (p.Ala71=) rs767759337 0.00019
NM_052945.4(TNFRSF13C):c.181G>A (p.Glu61Lys) rs1052712048 0.00006
NM_052945.4(TNFRSF13C):c.307C>A (p.Arg103=) rs369626832 0.00004
NM_052945.4(TNFRSF13C):c.224C>A (p.Pro75His) rs766314604 0.00003
NM_052945.4(TNFRSF13C):c.101C>A (p.Ala34Asp) rs777204893 0.00001
NM_052945.4(TNFRSF13C):c.165G>A (p.Thr55=) rs886057590 0.00001
NM_052945.4(TNFRSF13C):c.190G>A (p.Gly64Ser) rs1439217837 0.00001
NM_052945.4(TNFRSF13C):c.199G>A (p.Ala67Thr) rs1050585658 0.00001
NM_052945.4(TNFRSF13C):c.226G>T (p.Gly76Trp) rs1037657715 0.00001
NM_052945.4(TNFRSF13C):c.238G>A (p.Gly80Ser) rs747671330 0.00001
NM_052945.4(TNFRSF13C):c.264_265insATGGTCCTGGCG (p.Ala88_Leu89insMetValLeuAla) rs2077629096 0.00001
NM_052945.4(TNFRSF13C):c.288G>A (p.Val96=) rs755167957 0.00001
NM_052945.4(TNFRSF13C):c.35A>G (p.Asp12Gly) rs1215819338 0.00001
NM_052945.4(TNFRSF13C):c.89G>A (p.Arg30His) rs1334352355 0.00001
NM_052945.4(TNFRSF13C):c.-10C>A rs886057591
NM_052945.4(TNFRSF13C):c.101C>T (p.Ala34Val)
NM_052945.4(TNFRSF13C):c.11G>A (p.Gly4Glu) rs2077635455
NM_052945.4(TNFRSF13C):c.11G>C (p.Gly4Ala)
NM_052945.4(TNFRSF13C):c.122C>T (p.Pro41Leu) rs1556159000
NM_052945.4(TNFRSF13C):c.128C>T (p.Pro43Leu) rs2077634246
NM_052945.4(TNFRSF13C):c.134C>G (p.Pro45Arg)
NM_052945.4(TNFRSF13C):c.134C>T (p.Pro45Leu) rs1028425566
NM_052945.4(TNFRSF13C):c.142G>A (p.Ala48Thr) rs1407623179
NM_052945.4(TNFRSF13C):c.149G>A (p.Ser50Asn)
NM_052945.4(TNFRSF13C):c.14C>A (p.Pro5His) rs921374310
NM_052945.4(TNFRSF13C):c.173A>T (p.Gln58Leu) rs1602373983
NM_052945.4(TNFRSF13C):c.196_213del (p.Gly66_Ala71del)
NM_052945.4(TNFRSF13C):c.199G>T (p.Ala67Ser)
NM_052945.4(TNFRSF13C):c.202G>A (p.Gly68Ser)
NM_052945.4(TNFRSF13C):c.209C>T (p.Ala70Val) rs1234917601
NM_052945.4(TNFRSF13C):c.224C>T (p.Pro75Leu)
NM_052945.4(TNFRSF13C):c.244C>T (p.Pro82Ser)
NM_052945.4(TNFRSF13C):c.245C>T (p.Pro82Leu) rs2077629301
NM_052945.4(TNFRSF13C):c.255G>C (p.Leu85=) rs544076556
NM_052945.4(TNFRSF13C):c.257G>T (p.Gly86Val)
NM_052945.4(TNFRSF13C):c.257_268del (p.Gly86_Leu89del) rs745586116
NM_052945.4(TNFRSF13C):c.25C>T (p.Arg9Trp)
NM_052945.4(TNFRSF13C):c.264_275dup (p.88ALVL[3]) rs776259962
NM_052945.4(TNFRSF13C):c.275_286del (p.88ALVL[1]) rs770676417
NM_052945.4(TNFRSF13C):c.275_286dup (p.88ALVL[3]) rs770676417
NM_052945.4(TNFRSF13C):c.278T>C (p.Leu93Pro) rs2077628911
NM_052945.4(TNFRSF13C):c.289G>A (p.Gly97Ser)
NM_052945.4(TNFRSF13C):c.295G>C (p.Val99Leu)
NM_052945.4(TNFRSF13C):c.29G>A (p.Gly10Asp)
NM_052945.4(TNFRSF13C):c.2T>A (p.Met1Lys) rs1299112321
NM_052945.4(TNFRSF13C):c.311_322del (p.Arg104_Arg107del) rs1382035439
NM_052945.4(TNFRSF13C):c.325C>T (p.Arg109Cys) rs776189874
NM_052945.4(TNFRSF13C):c.326GCG[3] (p.Gly110dup) rs746833484
NM_052945.4(TNFRSF13C):c.331G>T (p.Ala111Ser) rs2146589165
NM_052945.4(TNFRSF13C):c.37G>T (p.Ala13Ser) rs2077635069
NM_052945.4(TNFRSF13C):c.46C>G (p.Pro16Ala)
NM_052945.4(TNFRSF13C):c.52C>T (p.Pro18Ser)
NM_052945.4(TNFRSF13C):c.5G>A (p.Arg2Lys)
NM_052945.4(TNFRSF13C):c.68A>G (p.Glu23Gly)
NM_052945.4(TNFRSF13C):c.85G>A (p.Val29Ile)

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