ClinVar Miner

List of variants in gene FADD reported as uncertain significance for immune system disorder

Included ClinVar conditions (908):
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Gene type:
ClinVar version:
Total variants: 45
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HGVS dbSNP gnomAD frequency
NM_003824.4(FADD):c.439A>G (p.Ile147Val) rs140822085 0.00012
NM_003824.4(FADD):c.452C>T (p.Thr151Ile) rs150178083 0.00011
NM_003824.4(FADD):c.313T>C (p.Cys105Arg) rs369869993 0.00006
NM_003824.4(FADD):c.307G>A (p.Val103Ile) rs200845739 0.00004
NM_003824.4(FADD):c.31G>A (p.Val11Met) rs753665798 0.00002
NM_003824.4(FADD):c.466G>A (p.Ala156Thr) rs767771723 0.00002
NM_003824.4(FADD):c.52A>C (p.Ser18Arg) rs1408886315 0.00002
NM_003824.4(FADD):c.304A>C (p.Asn102His) rs1437990933 0.00001
NM_003824.4(FADD):c.324G>A (p.Val108=) rs41269121 0.00001
NM_003824.4(FADD):c.385A>G (p.Ile129Val) rs750867105 0.00001
NM_003824.4(FADD):c.419G>A (p.Arg140His) rs1371367785 0.00001
NM_003824.4(FADD):c.547G>T (p.Ala183Ser) rs763073852 0.00001
NM_003824.4(FADD):c.551G>A (p.Arg184His) rs145623767 0.00001
NM_003824.4(FADD):c.8C>G (p.Pro3Arg) rs763339860 0.00001
NM_003824.4(FADD):c.109G>A (p.Glu37Lys)
NM_003824.4(FADD):c.139T>A (p.Ser47Thr)
NM_003824.4(FADD):c.152A>G (p.Glu51Gly) rs2049438451
NM_003824.4(FADD):c.168G>T (p.Glu56Asp) rs777501231
NM_003824.4(FADD):c.175C>T (p.His59Tyr)
NM_003824.4(FADD):c.206C>T (p.Ser69Phe)
NM_003824.4(FADD):c.241G>T (p.Asp81Tyr) rs2049439412
NM_003824.4(FADD):c.306C>G (p.Asn102Lys) rs775250989
NM_003824.4(FADD):c.310A>G (p.Ile104Val) rs2135899812
NM_003824.4(FADD):c.316G>A (p.Asp106Asn)
NM_003824.4(FADD):c.330A>C (p.Lys110Asn) rs2135899832
NM_003824.4(FADD):c.334T>G (p.Trp112Gly)
NM_003824.4(FADD):c.349C>T (p.Arg117Cys)
NM_003824.4(FADD):c.350G>A (p.Arg117His) rs1392069885
NM_003824.4(FADD):c.359A>G (p.Lys120Arg)
NM_003824.4(FADD):c.378C>G (p.Ile126Met) rs61757382
NM_003824.4(FADD):c.382A>G (p.Ser128Gly)
NM_003824.4(FADD):c.397T>C (p.Tyr133His) rs2049458420
NM_003824.4(FADD):c.416A>G (p.Glu139Gly)
NM_003824.4(FADD):c.475G>A (p.Ala159Thr) rs1555063819
NM_003824.4(FADD):c.508A>T (p.Met170Leu)
NM_003824.4(FADD):c.513C>A (p.Asn171Lys)
NM_003824.4(FADD):c.51C>G (p.Ser17Arg) rs1441791156
NM_003824.4(FADD):c.52A>G (p.Ser18Gly) rs1408886315
NM_003824.4(FADD):c.541C>G (p.Gln181Glu)
NM_003824.4(FADD):c.578T>C (p.Met193Thr)
NM_003824.4(FADD):c.584C>T (p.Pro195Leu) rs1194936880
NM_003824.4(FADD):c.604G>A (p.Ala202Thr) rs1313312609
NM_003824.4(FADD):c.617A>C (p.Glu206Ala) rs2135900115
NM_003824.4(FADD):c.623C>T (p.Ser208Phe) rs2135900136
NM_003824.4(FADD):c.89G>C (p.Arg30Pro) rs369187743

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