ClinVar Miner

List of variants reported as uncertain significance for Hereditary Paraganglioma-Pheochromocytoma Syndromes by Illumina Clinical Services Laboratory,Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 80
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HGVS dbSNP
NC_000011.10:g.61430118G>A
NM_001035511.2(SDHC):c.*1052C>T
NM_001035511.2(SDHC):c.*1074G>T
NM_001035511.2(SDHC):c.*1543A>C
NM_001035511.2(SDHC):c.*1913A>G
NM_001035511.2(SDHC):c.*2133C>A
NM_001035511.2(SDHC):c.*748C>T
NM_001035511.2(SDHC):c.*763G>C
NM_001035511.2(SDHC):c.*945G>C
NM_003000.2(SDHB):c.*102A>G rs201155896
NM_003000.2(SDHB):c.*133T>C rs111686611
NM_003000.2(SDHB):c.-135G>A rs886045587
NM_003000.2(SDHB):c.-142A>G rs886045588
NM_003000.2(SDHB):c.299C>G (p.Ser100Cys) rs121917755
NM_003000.2(SDHB):c.344G>A (p.Arg115Gln) rs200973284
NM_003000.2(SDHB):c.395A>G (p.His132Arg) rs74315372
NM_003000.2(SDHB):c.454T>C (p.Ser152Pro) rs886045584
NM_003000.2(SDHB):c.65G>T (p.Cys22Phe) rs141230910
NM_003000.2(SDHB):c.716C>T (p.Ser239Phe) rs201098090
NM_003000.3(SDHB):c.540+8G>T
NM_003001.3(SDHC):c.*1889T>C rs746551127
NM_003001.3(SDHC):c.*1918G>A rs867593097
NM_003001.3(SDHC):c.*2274G>A rs886045497
NM_003001.3(SDHC):c.*780G>A rs886045483
NM_003001.3(SDHC):c.*863G>A rs570400725
NM_003001.5(SDHC):c.*115T>G rs886045478
NM_003001.5(SDHC):c.*174G>A rs886045479
NM_003001.5(SDHC):c.*251C>T rs886045480
NM_003001.5(SDHC):c.*252G>A
NM_003001.5(SDHC):c.*34A>G rs886045477
NM_003001.5(SDHC):c.*409G>A rs186995249
NM_003001.5(SDHC):c.*540A>G
NM_003001.5(SDHC):c.*632A>G rs886045482
NM_003001.5(SDHC):c.*707G>A
NM_003001.5(SDHC):c.*728C>G
NM_003001.5(SDHC):c.*773A>G
NM_003001.5(SDHC):c.128A>G (p.Asn43Ser) rs747349777
NM_003001.5(SDHC):c.15G>T (p.Leu5Phe) rs771746264
NM_003001.5(SDHC):c.54T>G (p.Phe18Leu) rs200761743
NM_003002.4(SDHD):c.*111A>G
NM_003002.4(SDHD):c.*302A>G rs201163059
NM_003002.4(SDHD):c.*587A>G rs886047701
NM_003002.4(SDHD):c.*648A>G rs201560447
NM_003002.4(SDHD):c.*663A>G rs200264243
NM_003002.4(SDHD):c.*669T>C
NM_003002.4(SDHD):c.*71C>A rs886047700
NM_003002.4(SDHD):c.*738T>A rs886047702
NM_003002.4(SDHD):c.*762A>G
NM_003002.4(SDHD):c.*815T>C rs886047703
NM_003002.4(SDHD):c.*93A>G
NM_003002.4(SDHD):c.136G>A (p.Val46Met) rs886047699
NM_003002.4(SDHD):c.174C>T (p.Gly58=)
NM_003002.4(SDHD):c.228C>T (p.Leu76=) rs148634289
NM_003002.4(SDHD):c.281C>G (p.Ser94Cys) rs199754684
NM_003002.4(SDHD):c.445A>G (p.Ile149Val)
NM_003002.4(SDHD):c.53-6C>A
NM_004168.4(SDHA):c.*102G>A
NM_004168.4(SDHA):c.*179G>A
NM_004168.4(SDHA):c.*189C>T rs185107377
NM_004168.4(SDHA):c.*75A>G rs886060517
NM_004168.4(SDHA):c.1014G>A (p.Ala338=) rs201341132
NM_004168.4(SDHA):c.1092C>T (p.Val364=) rs886060515
NM_004168.4(SDHA):c.1527G>A (p.Ser509=) rs746453879
NM_004168.4(SDHA):c.1727T>C (p.Leu576Pro) rs1318046349
NM_004168.4(SDHA):c.1969G>C (p.Val657Leu)
NM_004168.4(SDHA):c.269T>C (p.Val90Ala) rs886060514
NM_004168.4(SDHA):c.403G>A (p.Asp135Asn)
NM_004168.4(SDHA):c.512G>A (p.Arg171His) rs587782076
NM_004168.4(SDHA):c.583C>T (p.Arg195Trp)
NM_004168.4(SDHA):c.896-11G>T
NM_017841.2(SDHAF2):c.*233C>T rs886048419
NM_017841.2(SDHAF2):c.*389C>T rs886048420
NM_017841.2(SDHAF2):c.*446C>G rs886048421
NM_017841.2(SDHAF2):c.*58G>A rs754124809
NM_017841.2(SDHAF2):c.*669A>G rs747631379
NM_017841.2(SDHAF2):c.330C>A (p.Asn110Lys) rs779335034
NM_017841.4(SDHAF2):c.*284C>T
NM_017841.4(SDHAF2):c.*476C>T
NM_017841.4(SDHAF2):c.*479A>G
NM_017841.4(SDHAF2):c.*661A>G

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