ClinVar Miner

List of variants reported as benign for cardiovascular organ benign neoplasm

Included ClinVar conditions (43):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 62
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HGVS dbSNP
GRCh37/hg19 8q23.3(chr8:114378494-114450308)
NM_002253.3(KDR):c.3848+15T>C rs2412617
NM_002382.5(MAX):c.*1127G>C rs4902357
NM_002382.5(MAX):c.*404C>T rs4902359
NM_002382.5(MAX):c.*461C>T rs183428804
NM_002382.5(MAX):c.*565G>A rs1957948
NM_002382.5(MAX):c.*587G>A rs1957949
NM_002382.5(MAX):c.*717T>C rs4902358
NM_002382.5(MAX):c.*92G>A rs45604339
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.18C>A (p.Ala6=) rs2746462
NM_003000.2(SDHB):c.24C>T (p.Ser8=) rs148738139
NM_003000.2(SDHB):c.300T>C (p.Ser100=) rs11541235
NM_003000.2(SDHB):c.423+20T>A rs190139590
NM_003000.2(SDHB):c.424-37TTC[10] rs34261028
NM_003000.2(SDHB):c.487T>C (p.Ser163Pro) rs33927012
NM_003000.2(SDHB):c.8C>G (p.Ala3Gly) rs11203289
NM_003001.3(SDHC):c.*1025G>T rs16832859
NM_003001.3(SDHC):c.*1181_*1182insA rs34067216
NM_003001.3(SDHC):c.*123C>G rs3813632
NM_003001.3(SDHC):c.*1335A>G rs3935401
NM_003001.3(SDHC):c.*1379C>T rs114731359
NM_003001.3(SDHC):c.*1800G>C rs72714988
NM_003001.3(SDHC):c.*2052C>G rs12239492
NM_003001.3(SDHC):c.*2156A>C rs116668612
NM_003001.3(SDHC):c.*2318del rs57914150
NM_003001.3(SDHC):c.*247C>G rs540126021
NM_003001.3(SDHC):c.*385G>A rs8266
NM_003001.3(SDHC):c.*469G>A rs148834287
NM_003001.3(SDHC):c.*612C>T rs16865495
NM_003001.3(SDHC):c.*624A>G rs114438179
NM_003001.3(SDHC):c.*968A>G rs4600063
NM_003001.3(SDHC):c.-32T>C rs115782155
NM_003001.3(SDHC):c.-38G>A rs112556972
NM_003001.3(SDHC):c.20+11_20+12dup rs35215598
NM_003002.4(SDHD):c.*260T>A rs149570245
NM_003002.4(SDHD):c.*532A>T rs146261846
NM_003002.4(SDHD):c.*613T>C rs693441
NM_003002.4(SDHD):c.*803A>G rs17113461
NM_003002.4(SDHD):c.149A>G (p.His50Arg) rs11214077
NM_003002.4(SDHD):c.204C>T (p.Ser68=) rs9919552
NM_003002.4(SDHD):c.312C>T (p.His104=) rs61734352
NM_003002.4(SDHD):c.34G>A (p.Gly12Ser) rs34677591
NM_015074.3(KIF1B):c.*2042C>T rs1536262
NM_015074.3(KIF1B):c.*2247G>A rs1002076
NM_015074.3(KIF1B):c.*279_*280delCA rs111663673
NM_015074.3(KIF1B):c.*3911A>G rs1138791
NM_015074.3(KIF1B):c.*5019T>C rs3748581
NM_015074.3(KIF1B):c.1639+10C>T rs3753037
NM_015074.3(KIF1B):c.285C>G (p.Ala95=) rs12402052
NM_015074.3(KIF1B):c.5163C>A (p.Thr1721=) rs11121552
NM_017841.2(SDHAF2):c.*377T>C rs17702
NM_017841.2(SDHAF2):c.*378G>A rs7935377
NM_017841.2(SDHAF2):c.*415A>G rs61132686
NM_017841.2(SDHAF2):c.*456A>G rs6632
NM_017849.3(TMEM127):c.*1301T>C rs3770239
NM_017849.3(TMEM127):c.*1958A>C rs7058
NM_017849.3(TMEM127):c.621G>A (p.Ala207=) rs3852673
NM_020630.5(RET):c.-200A>G rs10900296
NM_020975.6(RET):c.*1506G>A rs2742241
NM_020975.6(RET):c.1296A>G (p.Ala432=) rs1800860

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