ClinVar Miner

List of variants in gene SDHB reported as likely benign for benign endocrine neoplasm

Included ClinVar conditions (23):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 153
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HGVS dbSNP
NM_003000.2(SDHB):c.113G>A (p.Arg38His) rs143058777
NM_003000.2(SDHB):c.144C>T (p.Asp48=) rs1553178737
NM_003000.2(SDHB):c.15C>A (p.Val5=) rs1182998682
NM_003000.2(SDHB):c.171T>C (p.His57=) rs1280868219
NM_003000.2(SDHB):c.21C>G (p.Leu7=) rs147815442
NM_003000.2(SDHB):c.225T>C (p.Ala75=) rs201762207
NM_003000.2(SDHB):c.264C>G (p.Thr88=) rs41310416
NM_003000.2(SDHB):c.287-4T>C rs200419171
NM_003000.2(SDHB):c.306A>G (p.Ala102=) rs1553177766
NM_003000.2(SDHB):c.312C>T (p.Asn104=) rs876660346
NM_003000.2(SDHB):c.339C>T (p.Cys113=) rs754582722
NM_003000.2(SDHB):c.33C>T (p.Arg11=) rs146399542
NM_003000.2(SDHB):c.357C>T (p.Thr119=) rs1553177749
NM_003000.2(SDHB):c.42G>A (p.Pro14=) rs760753435
NM_003000.2(SDHB):c.465T>C (p.Pro155=) rs1553177685
NM_003000.2(SDHB):c.468T>C (p.Tyr156=) rs199718947
NM_003000.2(SDHB):c.480G>A (p.Lys160=) rs1553177683
NM_003000.2(SDHB):c.516G>A (p.Gln172=) rs138937650
NM_003000.2(SDHB):c.541-10C>T rs200004039
NM_003000.2(SDHB):c.541-6A>G rs1195530396
NM_003000.2(SDHB):c.541-7C>T rs201558574
NM_003000.2(SDHB):c.541-9C>T rs755367242
NM_003000.2(SDHB):c.543C>T (p.Asp181=) rs199809975
NM_003000.2(SDHB):c.549C>T (p.Leu183=) rs1411654404
NM_003000.2(SDHB):c.552C>T (p.Tyr184=) rs202098600
NM_003000.2(SDHB):c.588C>T (p.Cys196=) rs1060505015
NM_003000.2(SDHB):c.606C>T (p.Asn202=) rs199653121
NM_003000.2(SDHB):c.627T>C (p.Pro209=) rs1060505016
NM_003000.2(SDHB):c.642+10T>C rs780427803
NM_003000.2(SDHB):c.642+7T>C rs747423037
NM_003000.2(SDHB):c.65G>C (p.Cys22Ser) rs141230910
NM_003000.2(SDHB):c.66C>T (p.Cys22=) rs772853861
NM_003000.2(SDHB):c.696C>T (p.Ala232=) rs779143585
NM_003000.2(SDHB):c.700C>T (p.Leu234=) rs201728852
NM_003000.2(SDHB):c.72+7C>A rs1553179311
NM_003000.2(SDHB):c.720A>G (p.Leu240=) rs759446340
NM_003000.2(SDHB):c.723C>T (p.Tyr241=) rs878854583
NM_003000.2(SDHB):c.73-10A>C rs376494419
NM_003000.2(SDHB):c.765+8G>A rs1553177265
NM_003000.2(SDHB):c.766-6T>C rs1553176984
NM_003000.2(SDHB):c.768T>C (p.Gly256=) rs1060505017
NM_003000.2(SDHB):c.783A>G (p.Lys261=) rs1060505014
NM_003000.2(SDHB):c.816C>G (p.Thr272=) rs1454454086
NM_003000.3(SDHB):c.120G>A (p.Lys40=) rs1570958090
NM_003000.3(SDHB):c.123A>G (p.Lys41=)
NM_003000.3(SDHB):c.12G>A (p.Val4=) rs768683606
NM_003000.3(SDHB):c.138A>T (p.Arg46=)
NM_003000.3(SDHB):c.147A>G (p.Pro49=)
NM_003000.3(SDHB):c.15C>G (p.Val5=)
NM_003000.3(SDHB):c.15C>T (p.Val5=) rs1182998682
NM_003000.3(SDHB):c.162C>T (p.Asp54=)
NM_003000.3(SDHB):c.180T>A (p.Thr60=)
NM_003000.3(SDHB):c.183T>C (p.Tyr61=)
NM_003000.3(SDHB):c.18C>T (p.Ala6=)
NM_003000.3(SDHB):c.200+7A>G rs371329778
NM_003000.3(SDHB):c.201-6T>C
NM_003000.3(SDHB):c.201-7T>G
NM_003000.3(SDHB):c.201-9C>T
NM_003000.3(SDHB):c.216A>G (p.Val72=) rs1570951479
NM_003000.3(SDHB):c.217T>C (p.Leu73=)
NM_003000.3(SDHB):c.21C>A (p.Leu7=) rs147815442
NM_003000.3(SDHB):c.234G>A (p.Lys78=)
NM_003000.3(SDHB):c.243T>C (p.Asn81=)
NM_003000.3(SDHB):c.252C>T (p.Asp84=)
NM_003000.3(SDHB):c.25T>C (p.Leu9=) rs1060503768
NM_003000.3(SDHB):c.267C>T (p.Phe89=) rs1553178042
NM_003000.3(SDHB):c.279C>T (p.Cys93=)
NM_003000.3(SDHB):c.27G>A (p.Leu9=)
NM_003000.3(SDHB):c.286+8T>C
NM_003000.3(SDHB):c.287-7C>G
NM_003000.3(SDHB):c.287-9C>G
NM_003000.3(SDHB):c.303T>C (p.Cys101=)
NM_003000.3(SDHB):c.32G>A (p.Arg11His) rs111430410
NM_003000.3(SDHB):c.330T>C (p.Thr110=)
NM_003000.3(SDHB):c.336T>C (p.Ala112=)
NM_003000.3(SDHB):c.342C>T (p.Thr114=) rs528599830
NM_003000.3(SDHB):c.34C>A (p.Arg12=) rs761996626
NM_003000.3(SDHB):c.351T>A (p.Ile117=)
NM_003000.3(SDHB):c.36G>A (p.Arg12=)
NM_003000.3(SDHB):c.39G>A (p.Leu13=) rs201745731
NM_003000.3(SDHB):c.402T>C (p.Tyr134=)
NM_003000.3(SDHB):c.417T>C (p.Leu139=) rs1570948513
NM_003000.3(SDHB):c.423+7T>C
NM_003000.3(SDHB):c.423+8T>G
NM_003000.3(SDHB):c.423+9C>G
NM_003000.3(SDHB):c.423+9C>T rs1570948499
NM_003000.3(SDHB):c.424-17_424-9del
NM_003000.3(SDHB):c.424-4A>G
NM_003000.3(SDHB):c.424-6C>T
NM_003000.3(SDHB):c.424-6dup
NM_003000.3(SDHB):c.424-7A>C rs1570948064
NM_003000.3(SDHB):c.424-7A>T
NM_003000.3(SDHB):c.447G>A (p.Gln149=) rs200353146
NM_003000.3(SDHB):c.453A>G (p.Lys151=) rs1570947967
NM_003000.3(SDHB):c.45C>T (p.Ala15=) rs764875162
NM_003000.3(SDHB):c.477G>A (p.Lys159=)
NM_003000.3(SDHB):c.48A>C (p.Thr16=) rs1570963474
NM_003000.3(SDHB):c.501G>A (p.Lys167=) rs1570947881
NM_003000.3(SDHB):c.507G>A (p.Gln169=)
NM_003000.3(SDHB):c.519C>T (p.Ser173=)
NM_003000.3(SDHB):c.534G>A (p.Glu178=)
NM_003000.3(SDHB):c.540+8G>A
NM_003000.3(SDHB):c.541-18_541-8dup rs1553177448
NM_003000.3(SDHB):c.541-30_541-2dup
NM_003000.3(SDHB):c.541-5T>C
NM_003000.3(SDHB):c.541-7C>G
NM_003000.3(SDHB):c.54T>C (p.Leu18=) rs759446168
NM_003000.3(SDHB):c.54T>G (p.Leu18=)
NM_003000.3(SDHB):c.558C>T (p.Cys186=) rs1570945906
NM_003000.3(SDHB):c.564C>T (p.Leu188=)
NM_003000.3(SDHB):c.57C>T (p.Gly19=) rs1326601709
NM_003000.3(SDHB):c.582C>G (p.Thr194=) rs775450654
NM_003000.3(SDHB):c.582C>T (p.Thr194=) rs775450654
NM_003000.3(SDHB):c.597C>T (p.Tyr199=) rs1570945852
NM_003000.3(SDHB):c.609A>C (p.Gly203=) rs1570945818
NM_003000.3(SDHB):c.619C>T (p.Leu207=) rs1570945806
NM_003000.3(SDHB):c.624G>T (p.Gly208=) rs1214592422
NM_003000.3(SDHB):c.636T>C (p.Leu212=)
NM_003000.3(SDHB):c.63C>G (p.Ala21=) rs1557749647
NM_003000.3(SDHB):c.642+10T>A
NM_003000.3(SDHB):c.643-4C>G rs748796588
NM_003000.3(SDHB):c.643-4dup rs1570944969
NM_003000.3(SDHB):c.643-7T>C rs374921867
NM_003000.3(SDHB):c.643-8T>C
NM_003000.3(SDHB):c.645C>G (p.Ala215=)
NM_003000.3(SDHB):c.663C>T (p.Asp221=)
NM_003000.3(SDHB):c.678C>T (p.Phe226=) rs1570944907
NM_003000.3(SDHB):c.693G>A (p.Leu231=)
NM_003000.3(SDHB):c.711A>G (p.Pro237=)
NM_003000.3(SDHB):c.717T>A (p.Ser239=)
NM_003000.3(SDHB):c.717T>C (p.Ser239=)
NM_003000.3(SDHB):c.72+10G>A
NM_003000.3(SDHB):c.72+10G>C
NM_003000.3(SDHB):c.72+7C>T
NM_003000.3(SDHB):c.72+8C>G rs1570963404
NM_003000.3(SDHB):c.73-29del
NM_003000.3(SDHB):c.73-7A>C
NM_003000.3(SDHB):c.732C>T (p.His244=) rs1570944785
NM_003000.3(SDHB):c.738C>T (p.Ile246=) rs1476198465
NM_003000.3(SDHB):c.753G>A (p.Arg251=)
NM_003000.3(SDHB):c.762T>C (p.Pro254=)
NM_003000.3(SDHB):c.765+8G>T
NM_003000.3(SDHB):c.766-5T>C
NM_003000.3(SDHB):c.766-9T>G
NM_003000.3(SDHB):c.777A>T (p.Pro259=)
NM_003000.3(SDHB):c.789T>C (p.Ile263=) rs1395418494
NM_003000.3(SDHB):c.798C>T (p.Ile266=)
NM_003000.3(SDHB):c.828G>A (p.Lys276=)
NM_003000.3(SDHB):c.837A>G (p.Ser279=) rs770120161
NM_003000.3(SDHB):c.84A>G (p.Gly28=) rs1337602604
NM_003000.3(SDHB):c.93A>T (p.Thr31=)
NM_003000.3(SDHB):c.96T>G (p.Ala32=)
NM_003000.3(SDHB):c.9G>C (p.Ala3=)

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