List of variants in gene combination TNFSF12, TNFSF12-TNFSF13 reported as likely benign for Common variable immunodeficiency

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 74

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HGVS	dbSNP	gnomAD frequency
NM_003809.3(TNFSF12):c.357G>A (p.Gln119=)	rs147826685	0.00113
NM_003809.3(TNFSF12):c.450C>T (p.Ile150=)	rs147597489	0.00009
NM_003809.3(TNFSF12):c.690C>G (p.Pro230=)	rs1237382978	0.00009
NM_003809.3(TNFSF12):c.729C>T (p.Phe243=)	rs200770110	0.00007
NM_003809.3(TNFSF12):c.374-9C>T	rs367612596	0.00006
NM_003809.3(TNFSF12):c.373+18G>A	rs370242260	0.00005
NM_003809.3(TNFSF12):c.374-8G>A	rs551460083	0.00004
NM_003809.3(TNFSF12):c.159+15C>T	rs1274339400	0.00003
NM_003809.3(TNFSF12):c.141G>T (p.Arg47=)	rs1167726401	0.00002
NM_003809.3(TNFSF12):c.159+11G>T	rs1051286778	0.00002
NM_003809.3(TNFSF12):c.321C>T (p.Ile107=)	rs139642600	0.00002
NM_003809.3(TNFSF12):c.381C>T (p.Asp127=)	rs576803878	0.00002
NM_003809.3(TNFSF12):c.105C>G (p.Leu35=)	rs908438555	0.00001
NM_003809.3(TNFSF12):c.159+7C>A	rs535840017	0.00001
NM_003809.3(TNFSF12):c.208-7C>G	rs2070983662	0.00001
NM_003809.3(TNFSF12):c.318G>A (p.Ala106=)	rs764045774	0.00001
NM_003809.3(TNFSF12):c.337+12G>A	rs1367179093	0.00001
NM_003809.3(TNFSF12):c.337+14G>A	rs751618286	0.00001
NM_003809.3(TNFSF12):c.499-10C>T	rs1323154572	0.00001
NM_003809.3(TNFSF12):c.529C>T (p.Leu177=)	rs1239258225	0.00001
NM_003809.3(TNFSF12):c.663G>T (p.Gly221=)	rs776034989	0.00001
NM_003809.3(TNFSF12):c.105C>T (p.Leu35=)	rs908438555
NM_003809.3(TNFSF12):c.108C>T (p.Gly36=)	rs2150904074
NM_003809.3(TNFSF12):c.120C>T (p.Ala40=)
NM_003809.3(TNFSF12):c.147G>A (p.Ser49=)	rs1036232885
NM_003809.3(TNFSF12):c.159+7C>T	rs535840017
NM_003809.3(TNFSF12):c.160-14C>T
NM_003809.3(TNFSF12):c.160-16C>T
NM_003809.3(TNFSF12):c.160-21_160-17del
NM_003809.3(TNFSF12):c.186A>G (p.Ala62=)	rs2150904254
NM_003809.3(TNFSF12):c.207+10C>T
NM_003809.3(TNFSF12):c.207+11G>A	rs1266540123
NM_003809.3(TNFSF12):c.207+14G>A
NM_003809.3(TNFSF12):c.207+17G>A
NM_003809.3(TNFSF12):c.207+18C>T
NM_003809.3(TNFSF12):c.207+19G>A
NM_003809.3(TNFSF12):c.208-15C>T
NM_003809.3(TNFSF12):c.208-19C>G
NM_003809.3(TNFSF12):c.208-8T>A	rs2150904642
NM_003809.3(TNFSF12):c.219C>G (p.Pro73=)	rs2150904657
NM_003809.3(TNFSF12):c.243T>C (p.Pro81=)
NM_003809.3(TNFSF12):c.246G>A (p.Ala82=)
NM_003809.3(TNFSF12):c.249T>C (p.Pro83=)
NM_003809.3(TNFSF12):c.258C>T (p.Asn86=)
NM_003809.3(TNFSF12):c.288T>G (p.Pro96=)
NM_003809.3(TNFSF12):c.312A>G (p.Arg104=)	rs1326993093
NM_003809.3(TNFSF12):c.337+16G>A
NM_003809.3(TNFSF12):c.337+7G>A
NM_003809.3(TNFSF12):c.360C>T (p.Asp120=)
NM_003809.3(TNFSF12):c.366G>A (p.Ala122=)	rs529570679
NM_003809.3(TNFSF12):c.373+17C>T
NM_003809.3(TNFSF12):c.373+18G>T
NM_003809.3(TNFSF12):c.375T>G (p.Gly125=)
NM_003809.3(TNFSF12):c.384G>A (p.Gly128=)	rs1486694236
NM_003809.3(TNFSF12):c.393T>C (p.Ser131=)
NM_003809.3(TNFSF12):c.402G>A (p.Glu134=)
NM_003809.3(TNFSF12):c.417C>T (p.Asn139=)
NM_003809.3(TNFSF12):c.438C>T (p.Tyr146=)
NM_003809.3(TNFSF12):c.441C>T (p.Asn147=)	rs2150909109
NM_003809.3(TNFSF12):c.465C>T (p.Val155=)
NM_003809.3(TNFSF12):c.498+12C>G
NM_003809.3(TNFSF12):c.498+7C>T
NM_003809.3(TNFSF12):c.498+9del	rs1356188583
NM_003809.3(TNFSF12):c.499-4C>T	rs993444940
NM_003809.3(TNFSF12):c.535C>T (p.Leu179=)	rs2150909482
NM_003809.3(TNFSF12):c.573C>T (p.Cys191=)
NM_003809.3(TNFSF12):c.600G>A (p.Ala200=)
NM_003809.3(TNFSF12):c.609C>G (p.Leu203=)	rs140608168
NM_003809.3(TNFSF12):c.624C>A (p.Arg208=)
NM_003809.3(TNFSF12):c.651C>T (p.Ala217=)
NM_003809.3(TNFSF12):c.657G>A (p.Arg219=)
NM_003809.3(TNFSF12):c.657G>T (p.Arg219=)	rs1363429844
NM_003809.3(TNFSF12):c.673C>A (p.Arg225=)	rs761260715
NM_003809.3(TNFSF12):c.687C>T (p.Leu229=)

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