ClinVar Miner

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

Included ClinVar conditions (43):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 44
Download table as spreadsheet
HGVS dbSNP
NM_003000.2(SDHB):c.-139G>T rs114522228
NM_003000.2(SDHB):c.-37T>C rs143031690
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.158G>A (p.Gly53Glu) rs34916635
NM_003000.2(SDHB):c.170A>G (p.His57Arg) rs35962811
NM_003000.2(SDHB):c.171T>C (p.His57=) rs1280868219
NM_003000.2(SDHB):c.200+7A>G rs371329778
NM_003000.2(SDHB):c.21C>T (p.Leu7=) rs147815442
NM_003000.2(SDHB):c.225T>C (p.Ala75=) rs201762207
NM_003000.2(SDHB):c.24C>T (p.Ser8=) rs148738139
NM_003000.2(SDHB):c.287-4T>C rs200419171
NM_003000.2(SDHB):c.300T>C (p.Ser100=) rs11541235
NM_003000.2(SDHB):c.306A>G (p.Ala102=) rs1553177766
NM_003000.2(SDHB):c.32G>A (p.Arg11His) rs111430410
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.468T>C (p.Tyr156=) rs199718947
NM_003000.2(SDHB):c.480G>A (p.Lys160=) rs1553177683
NM_003000.2(SDHB):c.487T>C (p.Ser163Pro) rs33927012
NM_003000.2(SDHB):c.516G>A (p.Gln172=) rs138937650
NM_003000.2(SDHB):c.541-18_541-8dup rs1553177448
NM_003000.2(SDHB):c.541-6A>G rs1195530396
NM_003000.2(SDHB):c.541-7C>T rs201558574
NM_003000.2(SDHB):c.543C>T (p.Asp181=) rs199809975
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.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_003000.2(SDHB):c.8C>G (p.Ala3Gly) rs11203289

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.