ClinVar Miner

List of variants in gene SDHAF2 reported as likely benign by Invitae

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Gene type:
ClinVar version:
Total variants: 138
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HGVS dbSNP gnomAD frequency
NM_017841.4(SDHAF2):c.32C>T (p.Ser11Leu) rs148425779 0.00108
NM_017841.4(SDHAF2):c.319C>T (p.Arg107Cys) rs140191819 0.00067
NM_017841.4(SDHAF2):c.97C>T (p.Arg33Cys) rs144867876 0.00028
NM_017841.4(SDHAF2):c.15A>G (p.Thr5=) rs144511254 0.00014
NM_017841.4(SDHAF2):c.330C>T (p.Asn110=) rs779335034 0.00008
NM_017841.4(SDHAF2):c.37-18G>A rs374796679 0.00006
NM_017841.4(SDHAF2):c.24G>A (p.Ser8=) rs764251580 0.00005
NM_017841.4(SDHAF2):c.294A>G (p.Thr98=) rs762441285 0.00005
NM_017841.4(SDHAF2):c.370+8G>C rs764742919 0.00005
NM_017841.4(SDHAF2):c.465C>T (p.Ala155=) rs758154733 0.00005
NM_017841.4(SDHAF2):c.320G>A (p.Arg107His) rs535627239 0.00004
NM_017841.4(SDHAF2):c.371-12C>G rs771792041 0.00004
NM_017841.4(SDHAF2):c.315T>C (p.Tyr105=) rs750979204 0.00003
NM_017841.4(SDHAF2):c.370+17G>A rs1195374084 0.00003
NM_017841.4(SDHAF2):c.6G>A (p.Ala2=) rs747571875 0.00003
NM_017841.4(SDHAF2):c.99C>T (p.Arg33=) rs753325226 0.00003
NM_017841.4(SDHAF2):c.156G>A (p.Leu52=) rs773466310 0.00002
NM_017841.4(SDHAF2):c.371-4G>T rs775160119 0.00002
NM_017841.4(SDHAF2):c.207C>T (p.Arg69=) rs756825771 0.00001
NM_017841.4(SDHAF2):c.240G>A (p.Leu80=) rs1223446048 0.00001
NM_017841.4(SDHAF2):c.300G>A (p.Lys100=) rs1274218425 0.00001
NM_017841.4(SDHAF2):c.321C>T (p.Arg107=) rs754291669 0.00001
NM_017841.4(SDHAF2):c.324G>T (p.Leu108=) rs1426061764 0.00001
NM_017841.4(SDHAF2):c.36+19C>G rs780961861 0.00001
NM_017841.4(SDHAF2):c.36+6G>A rs1309376928 0.00001
NM_017841.4(SDHAF2):c.360C>T (p.Tyr120=) rs1328610836 0.00001
NM_017841.4(SDHAF2):c.387A>G (p.Pro129=) rs770383127 0.00001
NM_017841.4(SDHAF2):c.414C>T (p.Ala138=) rs766658781 0.00001
NM_017841.4(SDHAF2):c.450G>A (p.Glu150=) rs764146390 0.00001
NM_017841.4(SDHAF2):c.126T>C (p.Asp42=) rs1590764790
NM_017841.4(SDHAF2):c.12T>A (p.Ser4=) rs2135436188
NM_017841.4(SDHAF2):c.12T>C (p.Ser4=)
NM_017841.4(SDHAF2):c.132A>G (p.Gln44=) rs2134892277
NM_017841.4(SDHAF2):c.135G>A (p.Lys45=)
NM_017841.4(SDHAF2):c.138C>T (p.Asp46=) rs969049910
NM_017841.4(SDHAF2):c.153T>A (p.Pro51=)
NM_017841.4(SDHAF2):c.153T>G (p.Pro51=) rs769950627
NM_017841.4(SDHAF2):c.162A>G (p.Pro54=)
NM_017841.4(SDHAF2):c.171G>A (p.Glu57=) rs767436409
NM_017841.4(SDHAF2):c.180T>C (p.Asp60=) rs2134892368
NM_017841.4(SDHAF2):c.18G>A (p.Val6=) rs1590759621
NM_017841.4(SDHAF2):c.18G>C (p.Val6=)
NM_017841.4(SDHAF2):c.195C>T (p.Thr65=) rs2134892396
NM_017841.4(SDHAF2):c.198A>G (p.Lys66=) rs760482747
NM_017841.4(SDHAF2):c.216T>C (p.Tyr72=) rs778397152
NM_017841.4(SDHAF2):c.21C>T (p.Phe7=) rs892955355
NM_017841.4(SDHAF2):c.222C>T (p.Ser74=) rs749887667
NM_017841.4(SDHAF2):c.225A>G (p.Arg75=) rs2134892466
NM_017841.4(SDHAF2):c.228G>A (p.Lys76=) rs2134892475
NM_017841.4(SDHAF2):c.234A>G (p.Gly78=) rs2134892495
NM_017841.4(SDHAF2):c.249C>T (p.Cys83=) rs2134892531
NM_017841.4(SDHAF2):c.24G>T (p.Ser8=) rs764251580
NM_017841.4(SDHAF2):c.260+10T>C rs1590764949
NM_017841.4(SDHAF2):c.260+10T>G rs1590764949
NM_017841.4(SDHAF2):c.260+11A>C
NM_017841.4(SDHAF2):c.260+13G>A
NM_017841.4(SDHAF2):c.260+14A>T
NM_017841.4(SDHAF2):c.260+15G>A
NM_017841.4(SDHAF2):c.260+16T>C
NM_017841.4(SDHAF2):c.260+7G>C
NM_017841.4(SDHAF2):c.260+7G>T
NM_017841.4(SDHAF2):c.261-10T>C
NM_017841.4(SDHAF2):c.261-16T>C
NM_017841.4(SDHAF2):c.261-21_261-16del rs773213740
NM_017841.4(SDHAF2):c.261-8G>A rs779242759
NM_017841.4(SDHAF2):c.261-8G>C rs779242759
NM_017841.4(SDHAF2):c.261-9del rs1060504900
NM_017841.4(SDHAF2):c.264T>G (p.Leu88=) rs1554984669
NM_017841.4(SDHAF2):c.269C>T (p.Ala90Val) rs373951663
NM_017841.4(SDHAF2):c.270T>C (p.Ala90=)
NM_017841.4(SDHAF2):c.273A>G (p.Lys91=)
NM_017841.4(SDHAF2):c.288C>T (p.His96=) rs764919936
NM_017841.4(SDHAF2):c.294A>C (p.Thr98=) rs762441285
NM_017841.4(SDHAF2):c.30G>C (p.Ser10=) rs2135436336
NM_017841.4(SDHAF2):c.312C>A (p.Leu104=) rs1590765104
NM_017841.4(SDHAF2):c.324G>A (p.Leu108=) rs1426061764
NM_017841.4(SDHAF2):c.324G>C (p.Leu108=)
NM_017841.4(SDHAF2):c.327T>A (p.Ile109=) rs757670376
NM_017841.4(SDHAF2):c.33G>T (p.Ser11=)
NM_017841.4(SDHAF2):c.34C>T (p.Leu12=) rs2135436365
NM_017841.4(SDHAF2):c.354T>C (p.Ile118=) rs1590765153
NM_017841.4(SDHAF2):c.36+10G>C
NM_017841.4(SDHAF2):c.36+11A>C rs2135436466
NM_017841.4(SDHAF2):c.36+12G>A
NM_017841.4(SDHAF2):c.36+12G>C
NM_017841.4(SDHAF2):c.36+14A>G rs2135436481
NM_017841.4(SDHAF2):c.36+14A>T
NM_017841.4(SDHAF2):c.36+16G>A
NM_017841.4(SDHAF2):c.36+16G>T
NM_017841.4(SDHAF2):c.36+6GA[2] rs1157688980
NM_017841.4(SDHAF2):c.36+7A>G
NM_017841.4(SDHAF2):c.36+7_36+9del rs2135436444
NM_017841.4(SDHAF2):c.36+9A>T rs2135436453
NM_017841.4(SDHAF2):c.37-12T>C
NM_017841.4(SDHAF2):c.37-20T>C
NM_017841.4(SDHAF2):c.37-20T>G
NM_017841.4(SDHAF2):c.37-6T>C rs2134892037
NM_017841.4(SDHAF2):c.37-7A>G rs1554984610
NM_017841.4(SDHAF2):c.370+10A>G rs754379604
NM_017841.4(SDHAF2):c.370+10A>T
NM_017841.4(SDHAF2):c.370+12G>A rs886048415
NM_017841.4(SDHAF2):c.370+19A>C
NM_017841.4(SDHAF2):c.370+20G>T
NM_017841.4(SDHAF2):c.370+7G>C rs1590765180
NM_017841.4(SDHAF2):c.371-10T>C rs2134901887
NM_017841.4(SDHAF2):c.371-13T>A
NM_017841.4(SDHAF2):c.371-15_371-13del
NM_017841.4(SDHAF2):c.371-17C>G rs1404805808
NM_017841.4(SDHAF2):c.371-6T>C rs1467563046
NM_017841.4(SDHAF2):c.371-7C>G rs1277553449
NM_017841.4(SDHAF2):c.371-7C>T rs1277553449
NM_017841.4(SDHAF2):c.371-9C>G
NM_017841.4(SDHAF2):c.375T>C (p.Ala125=) rs1233830025
NM_017841.4(SDHAF2):c.378A>G (p.Lys126=)
NM_017841.4(SDHAF2):c.418C>T (p.Leu140=) rs2134902012
NM_017841.4(SDHAF2):c.420G>C (p.Leu140=) rs774723481
NM_017841.4(SDHAF2):c.421A>C (p.Arg141=) rs759780830
NM_017841.4(SDHAF2):c.432T>C (p.Ala144=)
NM_017841.4(SDHAF2):c.435A>G (p.Lys145=)
NM_017841.4(SDHAF2):c.453G>A (p.Gln151=) rs1271900425
NM_017841.4(SDHAF2):c.454A>C (p.Arg152=) rs1056273933
NM_017841.4(SDHAF2):c.456A>G (p.Arg152=) rs2134902088
NM_017841.4(SDHAF2):c.459G>C (p.Leu153=) rs757151603
NM_017841.4(SDHAF2):c.46C>T (p.Leu16=) rs1312422519
NM_017841.4(SDHAF2):c.471T>C (p.Asp157=)
NM_017841.4(SDHAF2):c.477G>A (p.Glu159=)
NM_017841.4(SDHAF2):c.483C>G (p.Leu161=) rs1862133729
NM_017841.4(SDHAF2):c.51A>C (p.Ser17=)
NM_017841.4(SDHAF2):c.51A>G (p.Ser17=) rs1590764718
NM_017841.4(SDHAF2):c.63A>T (p.Leu21=) rs191513932
NM_017841.4(SDHAF2):c.64T>C (p.Leu22=)
NM_017841.4(SDHAF2):c.66G>A (p.Leu22=) rs766468929
NM_017841.4(SDHAF2):c.69T>C (p.Ser23=)
NM_017841.4(SDHAF2):c.6G>T (p.Ala2=) rs747571875
NM_017841.4(SDHAF2):c.75G>A (p.Leu25=) rs2134892142
NM_017841.4(SDHAF2):c.90A>C (p.Ser30=)
NM_017841.4(SDHAF2):c.9G>A (p.Val3=) rs2135436159
NM_017841.4(SDHAF2):c.9G>C (p.Val3=)

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