ClinVar Miner

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

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ClinVar version:
Total variants: 22
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HGVS dbSNP
NC_000001.11:g.161314373C>T
NM_003000.2(SDHB):c.113G>A (p.Arg38His) rs143058777
NM_003000.2(SDHB):c.158G>A (p.Gly53Glu) rs34916635
NM_003000.2(SDHB):c.21C>T (p.Leu7=) rs147815442
NM_003000.2(SDHB):c.700C>T (p.Leu234=) rs201728852
NM_003000.3(SDHB):c.170A>G (p.His57Arg) rs35962811
NM_003000.3(SDHB):c.300T>C (p.Ser100=) rs11541235
NM_003001.5(SDHC):c.*78G>A rs182629842
NM_003001.5(SDHC):c.490A>T (p.Met164Leu) rs200375156
NM_003002.4(SDHD):c.118A>C (p.Ile40Leu) rs146276662
NM_003002.4(SDHD):c.53C>T (p.Ala18Val) rs192332761
NM_004168.4(SDHA):c.-1C>T rs560932680
NM_004168.4(SDHA):c.1177G>A (p.Val393Met) rs372989971
NM_004168.4(SDHA):c.163T>C (p.Tyr55His) rs142926807
NM_004168.4(SDHA):c.1680G>A (p.Thr560=) rs1139449
NM_004168.4(SDHA):c.1725G>A (p.Ala575=) rs758252610
NM_004168.4(SDHA):c.1886A>T (p.Tyr629Phe) rs6960
NM_004168.4(SDHA):c.1908+15C>T rs34504623
NM_004168.4(SDHA):c.1973C>T (p.Pro658Leu) rs377632619
NM_004168.4(SDHA):c.550G>A (p.Gly184Arg) rs148246073
NM_004168.4(SDHA):c.5C>T (p.Ser2Leu) rs780064103
NM_017841.2(SDHAF2):c.*12C>T rs113652589

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