ClinVar Miner

List of variants reported as likely benign for cardiovascular organ benign neoplasm by Invitae

Included ClinVar conditions (43):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 60
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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.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.287-4T>C rs200419171
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.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_003002.4(SDHD):c.114A>G (p.Arg38=) rs1555186794
NM_003002.4(SDHD):c.141G>A (p.Gln47=) rs1217254088
NM_003002.4(SDHD):c.159G>A (p.Pro53=) rs201368675
NM_003002.4(SDHD):c.170-10C>T rs952278127
NM_003002.4(SDHD):c.18G>A (p.Arg6=) rs200895313
NM_003002.4(SDHD):c.19C>T (p.Leu7=) rs1337542194
NM_003002.4(SDHD):c.21G>A (p.Leu7=) rs974401612
NM_003002.4(SDHD):c.228C>T (p.Leu76=) rs148634289
NM_003002.4(SDHD):c.270G>A (p.Ala90=) rs766656463
NM_003002.4(SDHD):c.270G>C (p.Ala90=) rs766656463
NM_003002.4(SDHD):c.27C>A (p.Ala9=) rs1555186670
NM_003002.4(SDHD):c.282C>G (p.Ser94=) rs781182616
NM_003002.4(SDHD):c.282C>T (p.Ser94=) rs781182616
NM_003002.4(SDHD):c.297C>T (p.Leu99=) rs749657880
NM_003002.4(SDHD):c.314+8T>C rs199645781
NM_003002.4(SDHD):c.315-9T>G rs911853469
NM_003002.4(SDHD):c.318C>A (p.Gly106=) rs878854592
NM_003002.4(SDHD):c.342T>C (p.Tyr114=) rs1050032491
NM_003002.4(SDHD):c.405C>A (p.Thr135=) rs1555187606
NM_003002.4(SDHD):c.42A>G (p.Leu14=) rs878854593
NM_003002.4(SDHD):c.435C>T (p.His145=) rs200062830
NM_003002.4(SDHD):c.53-6C>T rs757454290
NM_003002.4(SDHD):c.57G>A (p.Leu19=) rs560625389
NM_003002.4(SDHD):c.9T>A (p.Val3=) rs1555186657

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