ClinVar Miner

List of variants in gene TNFRSF1A reported by GeneDx

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Gene type:
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Total variants: 100
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HGVS dbSNP gnomAD frequency
NM_001065.4(TNFRSF1A):c.473-33T>C rs1800692 0.70815
NM_001065.3(TNFRSF1A):c.-610T>G rs4149570 0.69299
NM_001065.4(TNFRSF1A):c.36A>G (p.Pro12=) rs767455 0.39963
NM_001065.4(TNFRSF1A):c.625+10A>G rs1800693 0.38055
NM_001065.3(TNFRSF1A):c.-581A>G rs4149621 0.16099
NM_001065.4(TNFRSF1A):c.39+303A>G rs4149622 0.16098
NM_001065.4(TNFRSF1A):c.551+234A>G rs4149639 0.06168
NM_001065.3(TNFRSF1A):c.-383A>C rs2234649 0.04849
NM_001065.4(TNFRSF1A):c.769-55G>T rs4149645 0.02656
NM_001065.4(TNFRSF1A):c.769-56G>T rs4149644 0.02655
NM_001065.4(TNFRSF1A):c.40-305C>T rs58388160 0.02009
NM_001065.4(TNFRSF1A):c.40-217G>A rs77949925 0.01473
NM_001065.4(TNFRSF1A):c.362G>A (p.Arg121Gln) rs4149584 0.01206
NM_001065.4(TNFRSF1A):c.768+42del rs56222180 0.01198
NM_001065.4(TNFRSF1A):c.473-72G>A rs41309816 0.00730
NM_001065.4(TNFRSF1A):c.40-304T>C rs138345237 0.00647
NM_001065.4(TNFRSF1A):c.224C>T (p.Pro75Leu) rs4149637 0.00574
NM_001065.4(TNFRSF1A):c.194-29G>A rs74059209 0.00371
NM_001065.4(TNFRSF1A):c.40-208G>A rs74059210 0.00319
NM_001065.4(TNFRSF1A):c.472+64C>T rs4149585 0.00246
NM_001065.4(TNFRSF1A):c.1110C>T (p.Arg370=) rs201683984 0.00236
NM_001065.4(TNFRSF1A):c.935G>A (p.Arg312Lys) rs200900510 0.00113
NM_001065.4(TNFRSF1A):c.769-3C>T rs199743143 0.00054
NM_001065.4(TNFRSF1A):c.1075C>T (p.Leu359=) rs151344628 0.00050
NM_001065.4(TNFRSF1A):c.987C>T (p.Leu329=) rs138261783 0.00047
NM_001065.4(TNFRSF1A):c.193+6G>A rs147111217 0.00037
NM_001065.4(TNFRSF1A):c.369C>T (p.Thr123=) rs104895260 0.00036
NM_001065.4(TNFRSF1A):c.*64T>C rs200188649 0.00028
NM_001065.4(TNFRSF1A):c.1058-4G>A rs369451569 0.00026
NM_001065.4(TNFRSF1A):c.988G>A (p.Ala330Thr) rs200029309 0.00026
NM_001065.4(TNFRSF1A):c.645C>T (p.Pro215=) rs147075345 0.00020
NM_001065.4(TNFRSF1A):c.1206C>T (p.Ser402=) rs148334665 0.00018
NM_001065.4(TNFRSF1A):c.460G>A (p.Val154Met) rs201083197 0.00018
NM_001065.4(TNFRSF1A):c.194-14G>A rs104895241 0.00016
NM_001065.4(TNFRSF1A):c.147T>C (p.Tyr49=) rs150511666 0.00014
NM_001065.4(TNFRSF1A):c.1058-6C>G rs761155688 0.00011
NM_001065.4(TNFRSF1A):c.1328G>T (p.Gly443Val) rs201062001 0.00011
NM_001065.4(TNFRSF1A):c.459C>T (p.Thr153=) rs199792034 0.00011
NM_001065.4(TNFRSF1A):c.596T>C (p.Ile199Thr) rs104895247 0.00011
NM_001065.4(TNFRSF1A):c.249G>A (p.Glu83=) rs104895265 0.00010
NM_001065.4(TNFRSF1A):c.887G>C (p.Ser296Thr) rs770324989 0.00009
NM_001065.4(TNFRSF1A):c.334G>A (p.Val112Met) rs201753543 0.00007
NM_001065.4(TNFRSF1A):c.1197G>T (p.Ala399=) rs140486890 0.00006
NM_001065.4(TNFRSF1A):c.322+30G>A rs1046990537 0.00006
NM_001065.4(TNFRSF1A):c.551+22T>C rs199875984 0.00006
NM_001065.4(TNFRSF1A):c.168G>A (p.Ser56=) rs104895280 0.00005
NM_001065.4(TNFRSF1A):c.434A>G (p.Asn145Ser) rs104895288 0.00005
NM_001065.4(TNFRSF1A):c.1058-31G>A rs533012174 0.00004
NM_001065.4(TNFRSF1A):c.193+19G>A rs17847989 0.00003
NM_001065.4(TNFRSF1A):c.339G>A (p.Glu113=) rs587780965 0.00003
NM_001065.4(TNFRSF1A):c.492C>T (p.Thr164=) rs373422284 0.00003
NM_001065.4(TNFRSF1A):c.1002C>T (p.Ile334=) rs748720159 0.00002
NM_001065.4(TNFRSF1A):c.193+18C>T rs757177584 0.00002
NM_001065.4(TNFRSF1A):c.1012C>T (p.Leu338Phe) rs1251500082 0.00001
NM_001065.4(TNFRSF1A):c.16G>A (p.Val6Met) rs772424047 0.00001
NM_001065.4(TNFRSF1A):c.194-101C>T rs1948086341 0.00001
NM_001065.4(TNFRSF1A):c.194-111C>A rs987241172 0.00001
NM_001065.4(TNFRSF1A):c.370G>A (p.Val124Met) rs104895278 0.00001
NM_001065.4(TNFRSF1A):c.384G>A (p.Arg128=) rs747164054 0.00001
NM_001065.4(TNFRSF1A):c.482A>G (p.Lys161Arg) rs578112440 0.00001
NM_001065.4(TNFRSF1A):c.687C>A (p.Phe229Leu) rs766811013 0.00001
NM_001065.4(TNFRSF1A):c.894C>G (p.Thr298=) rs1057523965 0.00001
NM_001065.3(TNFRSF1A):c.-284delC rs140244212
NM_001065.3(TNFRSF1A):c.769-23_769-19delTTGCGinsCTGCT
NM_001065.4(TNFRSF1A):c.*22T>C rs759423059
NM_001065.4(TNFRSF1A):c.-55G>T rs201973707
NM_001065.4(TNFRSF1A):c.1057+16_1057+18del rs1455123790
NM_001065.4(TNFRSF1A):c.1058-58G>T rs1948008479
NM_001065.4(TNFRSF1A):c.1159C>T (p.Arg387Trp) rs1199072290
NM_001065.4(TNFRSF1A):c.1234C>G (p.Pro412Ala) rs876661181
NM_001065.4(TNFRSF1A):c.123T>G (p.Asp41Glu) rs104895271
NM_001065.4(TNFRSF1A):c.175T>C (p.Cys59Arg) rs104895217
NM_001065.4(TNFRSF1A):c.193+101G>A rs2136822905
NM_001065.4(TNFRSF1A):c.194-32C>T rs2136822779
NM_001065.4(TNFRSF1A):c.194-79G>A rs573219734
NM_001065.4(TNFRSF1A):c.219A>G (p.Pro73=) rs1469912868
NM_001065.4(TNFRSF1A):c.236C>T (p.Thr79Met) rs104895219
NM_001065.4(TNFRSF1A):c.242G>T (p.Cys81Phe) rs104895220
NM_001065.4(TNFRSF1A):c.265T>C (p.Phe89Leu) rs104895245
NM_001065.4(TNFRSF1A):c.282C>G (p.Asn94Lys) rs876661014
NM_001065.4(TNFRSF1A):c.287T>C (p.Leu96Pro) rs104895235
NM_001065.4(TNFRSF1A):c.295T>C (p.Cys99Arg) rs104895228
NM_001065.4(TNFRSF1A):c.305G>C (p.Cys102Ser) rs1555108112
NM_001065.4(TNFRSF1A):c.317G>A (p.Arg106Gln) rs876661031
NM_001065.4(TNFRSF1A):c.332A>G (p.Gln111Arg) rs2136822038
NM_001065.4(TNFRSF1A):c.343T>C (p.Ser115Pro) rs104895226
NM_001065.4(TNFRSF1A):c.40-268_40-267del rs528802948
NM_001065.4(TNFRSF1A):c.40-9C>A rs371080583
NM_001065.4(TNFRSF1A):c.472+47T>C rs371214815
NM_001065.4(TNFRSF1A):c.472+88C>A rs34567207
NM_001065.4(TNFRSF1A):c.473-4A>G rs2136821321
NM_001065.4(TNFRSF1A):c.551+13G>A rs2136821168
NM_001065.4(TNFRSF1A):c.626-32G>T rs200415260
NM_001065.4(TNFRSF1A):c.626-6C>T rs1275607339
NM_001065.4(TNFRSF1A):c.626-9T>C rs2136817455
NM_001065.4(TNFRSF1A):c.679C>G (p.Leu227Val)
NM_001065.4(TNFRSF1A):c.769-23= rs10849443
NM_001065.4(TNFRSF1A):c.769-55_769-54del rs1555107449
NM_001065.4(TNFRSF1A):c.806C>G (p.Pro269Arg) rs876661237
NM_001065.4(TNFRSF1A):c.959G>A (p.Gly320Glu) rs1057524143

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