ClinVar Miner

List of variants in gene TNFRSF1A reported as not provided for immune system disorder

Included ClinVar conditions (908):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 86
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HGVS dbSNP gnomAD frequency
NM_001065.4(TNFRSF1A):c.362G>A (p.Arg121Gln) rs4149584 0.01206
NM_001065.4(TNFRSF1A):c.552-89A>T rs104895264 0.00150
NM_001065.4(TNFRSF1A):c.39+97G>A rs151344626 0.00107
NM_001065.4(TNFRSF1A):c.1075C>T (p.Leu359=) rs151344628 0.00050
NM_001065.4(TNFRSF1A):c.369C>T (p.Thr123=) rs104895260 0.00036
NM_001065.4(TNFRSF1A):c.194-14G>A rs104895241 0.00016
NM_001065.4(TNFRSF1A):c.249G>A (p.Glu83=) rs104895265 0.00010
NM_001065.4(TNFRSF1A):c.473-16G>A rs104895251 0.00008
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_001065.2(TNFRSF1A):c.-559G>A rs151344625 0.00003
NM_001065.4(TNFRSF1A):c.194-15C>T rs104895259 0.00003
NM_001065.4(TNFRSF1A):c.228G>A (p.Gly76=) rs104895274 0.00002
NM_001065.4(TNFRSF1A):c.558G>A (p.Lys186=) rs104895275 0.00002
NM_001065.4(TNFRSF1A):c.283C>T (p.His95Tyr) rs104895290 0.00001
NM_001065.4(TNFRSF1A):c.370G>A (p.Val124Met) rs104895278 0.00001
NM_001065.4(TNFRSF1A):c.398G>A (p.Arg133Gln) rs104895257 0.00001
NM_001065.4(TNFRSF1A):c.1080C>G (p.Tyr360Ter) rs104895291
NM_001065.4(TNFRSF1A):c.123T>G (p.Asp41Glu) rs104895271
NM_001065.4(TNFRSF1A):c.145T>C (p.Tyr49His) rs104895237
NM_001065.4(TNFRSF1A):c.145T>G (p.Tyr49Asp) rs104895237
NM_001065.4(TNFRSF1A):c.151C>T (p.His51Tyr) rs104895227
NM_001065.4(TNFRSF1A):c.152A>G (p.His51Arg) rs104895289
NM_001065.4(TNFRSF1A):c.153C>G (p.His51Gln) rs104895254
NM_001065.4(TNFRSF1A):c.173G>A (p.Cys58Tyr) rs104895230
NM_001065.4(TNFRSF1A):c.173G>T (p.Cys58Phe) rs104895230
NM_001065.4(TNFRSF1A):c.175T>C (p.Cys59Arg) rs104895217
NM_001065.4(TNFRSF1A):c.176G>A (p.Cys59Tyr) rs104895223
NM_001065.4(TNFRSF1A):c.176G>C (p.Cys59Ser) rs104895223
NM_001065.4(TNFRSF1A):c.176G>T (p.Cys59Phe) rs104895223
NM_001065.4(TNFRSF1A):c.184T>G (p.Cys62Gly) rs104895225
NM_001065.4(TNFRSF1A):c.185G>A (p.Cys62Tyr) rs104895218
NM_001065.4(TNFRSF1A):c.194-18_194-17del rs104895267
NM_001065.4(TNFRSF1A):c.194G>A (p.Gly65Glu) rs104895239
NM_001065.4(TNFRSF1A):c.197C>T (p.Thr66Ile) rs104895243
NM_001065.4(TNFRSF1A):c.200A>C (p.Tyr67Ser) rs104895229
NM_001065.4(TNFRSF1A):c.200A>G (p.Tyr67Cys) rs104895229
NM_001065.4(TNFRSF1A):c.204G>C (p.Leu68Phe) rs104895262
NM_001065.4(TNFRSF1A):c.211_213del (p.Asp71del) rs104895246
NM_001065.4(TNFRSF1A):c.214T>C (p.Cys72Arg) rs104895238
NM_001065.4(TNFRSF1A):c.215G>A (p.Cys72Tyr) rs104895252
NM_001065.4(TNFRSF1A):c.215G>C (p.Cys72Ser) rs104895252
NM_001065.4(TNFRSF1A):c.236C>A (p.Thr79Lys) rs104895219
NM_001065.4(TNFRSF1A):c.236C>T (p.Thr79Met) rs104895219
NM_001065.4(TNFRSF1A):c.241T>C (p.Cys81Arg) rs104895232
NM_001065.4(TNFRSF1A):c.242G>A (p.Cys81Tyr) rs104895220
NM_001065.4(TNFRSF1A):c.242G>T (p.Cys81Phe) rs104895220
NM_001065.4(TNFRSF1A):c.243C>G (p.Cys81Trp) rs56002980
NM_001065.4(TNFRSF1A):c.250T>C (p.Cys84Arg) rs104895253
NM_001065.4(TNFRSF1A):c.251G>A (p.Cys84Tyr) rs104895224
NM_001065.4(TNFRSF1A):c.251G>C (p.Cys84Ser) rs104895224
NM_001065.4(TNFRSF1A):c.262T>C (p.Ser88Pro) rs104895292
NM_001065.4(TNFRSF1A):c.265T>C (p.Phe89Leu) rs104895245
NM_001065.4(TNFRSF1A):c.265T>G (p.Phe89Val) rs104895245
NM_001065.4(TNFRSF1A):c.266T>C (p.Phe89Ser) rs104895279
NM_001065.4(TNFRSF1A):c.267C>A (p.Phe89Leu) rs104895266
NM_001065.4(TNFRSF1A):c.269C>A (p.Thr90Asn) rs34751757
NM_001065.4(TNFRSF1A):c.281A>T (p.Asn94Ile) rs104895244
NM_001065.4(TNFRSF1A):c.284A>T (p.His95Leu) rs104895294
NM_001065.4(TNFRSF1A):c.287T>C (p.Leu96Pro) rs104895235
NM_001065.4(TNFRSF1A):c.293_295del (p.His98_Cys99delinsArg) rs104895261
NM_001065.4(TNFRSF1A):c.295T>A (p.Cys99Ser) rs104895228
NM_001065.4(TNFRSF1A):c.295T>C (p.Cys99Arg) rs104895228
NM_001065.4(TNFRSF1A):c.295T>G (p.Cys99Gly) rs104895228
NM_001065.4(TNFRSF1A):c.296G>A (p.Cys99Tyr) rs104895231
NM_001065.4(TNFRSF1A):c.304T>C (p.Cys102Arg) rs104895236
NM_001065.4(TNFRSF1A):c.306C>G (p.Cys102Trp) rs104895249
NM_001065.4(TNFRSF1A):c.308C>G (p.Ser103Cys) rs104895283
NM_001065.4(TNFRSF1A):c.323-32A>G rs104895281
NM_001065.4(TNFRSF1A):c.343T>C (p.Ser115Pro) rs104895226
NM_001065.4(TNFRSF1A):c.349T>C (p.Cys117Arg) rs104895221
NM_001065.4(TNFRSF1A):c.350G>A (p.Cys117Tyr) rs104895222
NM_001065.4(TNFRSF1A):c.361C>T (p.Arg121Trp) rs104895276
NM_001065.4(TNFRSF1A):c.362G>C (p.Arg121Pro) rs4149584
NM_001065.4(TNFRSF1A):c.374G>A (p.Cys125Tyr) rs104895234
NM_001065.4(TNFRSF1A):c.380G>A (p.Cys127Tyr) rs104895242
NM_001065.4(TNFRSF1A):c.40-981C>T rs151344627
NM_001065.4(TNFRSF1A):c.401A>C (p.His134Pro) rs104895284
NM_001065.4(TNFRSF1A):c.413A>C (p.Glu138Ala) rs104895286
NM_001065.4(TNFRSF1A):c.421T>A (p.Phe141Ile) rs104895233
NM_001065.4(TNFRSF1A):c.472+1G>A rs104895287
NM_001065.4(TNFRSF1A):c.472+6C>T rs104895277
NM_001065.4(TNFRSF1A):c.586_612del (p.Leu196_Gly204del) rs104895272
NM_001065.4(TNFRSF1A):c.596T>A (p.Ile199Asn) rs104895247
NM_001065.4(TNFRSF1A):c.605T>A (p.Val202Asp) rs104895285
NM_001065.4(TNFRSF1A):c.678C>G (p.Ser226=) rs104895258

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