ClinVar Miner

List of variants in gene ADA reported as likely pathogenic for T-B- severe combined immunodeficiency

Included ClinVar conditions (30):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 89
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HGVS dbSNP gnomAD frequency
NM_000022.4(ADA):c.986C>T (p.Ala329Val) rs121908715 0.00021
NM_000022.4(ADA):c.221G>T (p.Gly74Val) rs199422328 0.00009
NM_000022.4(ADA):c.632G>A (p.Arg211His) rs121908716 0.00009
NM_000022.4(ADA):c.320T>C (p.Leu107Pro) rs121908739 0.00007
NM_000022.4(ADA):c.757C>T (p.Arg253Trp) rs201944717 0.00005
NM_000022.4(ADA):c.872C>T (p.Ser291Leu) rs121908721 0.00005
NM_000022.4(ADA):c.715G>A (p.Gly239Ser) rs777820729 0.00003
NM_000022.4(ADA):c.890C>A (p.Pro297Gln) rs121908718 0.00003
NM_000022.4(ADA):c.350G>A (p.Trp117Ter) rs749484894 0.00002
NM_000022.4(ADA):c.454C>A (p.Leu152Met) rs121908728 0.00002
NM_000022.4(ADA):c.529G>A (p.Val177Met) rs121908719 0.00002
NM_000022.4(ADA):c.704G>A (p.Arg235Gln) rs79281338 0.00002
NM_000022.4(ADA):c.911T>G (p.Leu304Arg) rs199422327 0.00002
NM_000022.4(ADA):c.247G>A (p.Ala83Thr) rs776103734 0.00001
NM_000022.4(ADA):c.301C>T (p.Arg101Trp) rs121908717 0.00001
NM_000022.4(ADA):c.377C>A (p.Pro126Gln) rs1233957241 0.00001
NM_000022.4(ADA):c.445C>T (p.Arg149Trp) rs121908733 0.00001
NM_000022.4(ADA):c.466C>T (p.Arg156Cys) rs121908735 0.00001
NM_000022.4(ADA):c.467G>A (p.Arg156His) rs121908722 0.00001
NM_000022.4(ADA):c.536C>A (p.Ala179Asp) rs121908727 0.00001
NM_000022.4(ADA):c.631C>T (p.Arg211Cys) rs121908740 0.00001
NM_000022.4(ADA):c.780+1G>A rs746052951 0.00001
NM_000022.4(ADA):c.845+1G>C rs766590645 0.00001
NM_000022.4(ADA):c.845G>A (p.Arg282Gln) rs751635016 0.00001
NC_000020.10:g.(?_43255077)_(43264949_?)dup
NC_000020.11:g.(?_44636217)_(44636298_?)dup
NM_000022.3(ADA):c.[780+1G>A];[986C>T]
NM_000022.4(ADA):c.1078+1G>A
NM_000022.4(ADA):c.1078+2T>A rs1555843178
NM_000022.4(ADA):c.1078+2T>C
NM_000022.4(ADA):c.219-1G>A rs751147673
NM_000022.4(ADA):c.219-2A>G rs387906267
NM_000022.4(ADA):c.220G>T (p.Gly74Cys) rs121908730
NM_000022.4(ADA):c.221G>A (p.Gly74Asp)
NM_000022.4(ADA):c.293del (p.Val98fs)
NM_000022.4(ADA):c.301C>G (p.Arg101Gly) rs121908717
NM_000022.4(ADA):c.311C>T (p.Pro104Leu) rs1452483770
NM_000022.4(ADA):c.322del (p.Ala108fs)
NM_000022.4(ADA):c.362+5_362+8del rs763595926
NM_000022.4(ADA):c.363-1G>T
NM_000022.4(ADA):c.363-2A>G rs2145318314
NM_000022.4(ADA):c.363-2A>T
NM_000022.4(ADA):c.366_367del (p.Asp123fs) rs758073965
NM_000022.4(ADA):c.383_404dup (p.Leu137fs) rs1555844616
NM_000022.4(ADA):c.385G>A (p.Val129Met) rs121908731
NM_000022.4(ADA):c.385G>T (p.Val129Leu) rs121908731
NM_000022.4(ADA):c.396dup (p.Val133fs) rs1555844617
NM_000022.4(ADA):c.407del (p.Gly136fs)
NM_000022.4(ADA):c.410del (p.Leu137fs)
NM_000022.4(ADA):c.412C>T (p.Gln138Ter)
NM_000022.4(ADA):c.455T>C (p.Leu152Pro) rs1568845361
NM_000022.4(ADA):c.460T>C (p.Cys154Arg)
NM_000022.4(ADA):c.467G>C (p.Arg156Pro) rs121908722
NM_000022.4(ADA):c.478+1G>C
NM_000022.4(ADA):c.478+6T>C rs1555844600
NM_000022.4(ADA):c.479-23_479-2delinsTGGGACCAGCAT
NM_000022.4(ADA):c.479-2del rs1600921786
NM_000022.4(ADA):c.511A>T (p.Lys171Ter) rs2065361731
NM_000022.4(ADA):c.516C>A (p.Tyr172Ter) rs748810619
NM_000022.4(ADA):c.532del (p.Val177_Val178insTer) rs886041796
NM_000022.4(ADA):c.603C>A (p.Tyr201Ter) rs1555844395
NM_000022.4(ADA):c.603C>G (p.Tyr201Ter) rs1555844395
NM_000022.4(ADA):c.606+1G>T
NM_000022.4(ADA):c.622_632del (p.Gly208fs)
NM_000022.4(ADA):c.631C>A (p.Arg211Ser)
NM_000022.4(ADA):c.674_675del (p.Lys225fs)
NM_000022.4(ADA):c.679-2A>G
NM_000022.4(ADA):c.703C>T (p.Arg235Trp) rs778809577
NM_000022.4(ADA):c.716G>A (p.Gly239Asp) rs1312320956
NM_000022.4(ADA):c.755_756insTG (p.Arg253fs)
NM_000022.4(ADA):c.767del (p.Asn256fs) rs2123517868
NM_000022.4(ADA):c.780+1del rs2123517791
NM_000022.4(ADA):c.781-1G>T
NM_000022.4(ADA):c.785_786insGTCTG (p.Cys262fs) rs757796081
NM_000022.4(ADA):c.790del (p.Trp264fs) rs1555844006
NM_000022.4(ADA):c.791G>A (p.Trp264Ter) rs2065342571
NM_000022.4(ADA):c.813_814insAC (p.Trp272fs)
NM_000022.4(ADA):c.829del (p.Glu277fs)
NM_000022.4(ADA):c.845G>T (p.Arg282Leu)
NM_000022.4(ADA):c.854dup (p.Asn285fs) rs2123511347
NM_000022.4(ADA):c.859C>T (p.Gln287Ter) rs2065327852
NM_000022.4(ADA):c.872C>G (p.Ser291Trp) rs121908721
NM_000022.4(ADA):c.877_878delinsT (p.Asn293fs)
NM_000022.4(ADA):c.890C>T (p.Pro297Leu) rs121908718
NM_000022.4(ADA):c.906_915delinsTGTTACCAGATTACCAGATG (p.Thr303fs)
NM_000022.4(ADA):c.946_947insTGTT (p.Gly316fs)
NM_000022.4(ADA):c.956_960del (p.Glu319fs) rs771266745
NM_000022.4(ADA):c.976-1_979del rs1441174171
NM_000022.4(ADA):c.976-34G>A rs1194494050

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