ClinVar Miner

List of variants reported as benign for adrenal gland pheochromocytoma by Illumina Clinical Services Laboratory,Illumina

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 49
Download table as spreadsheet
HGVS dbSNP
NM_002382.4(MAX):c.*1127G>C rs4902357
NM_002382.4(MAX):c.*404C>T rs4902359
NM_002382.4(MAX):c.*461C>T rs183428804
NM_002382.4(MAX):c.*565G>A rs1957948
NM_002382.4(MAX):c.*587G>A rs1957949
NM_002382.4(MAX):c.*717T>C rs4902358
NM_002382.4(MAX):c.*92G>A rs45604339
NM_003000.2(SDHB):c.18C>A (p.Ala6=) rs2746462
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.*2311delA 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+12dupTG rs35215598
NM_003002.3(SDHD):c.*260T>A rs149570245
NM_003002.3(SDHD):c.*532A>T rs146261846
NM_003002.3(SDHD):c.*613T>C rs693441
NM_003002.3(SDHD):c.*803A>G rs17113461
NM_003002.3(SDHD):c.204C>T (p.Ser68=) rs9919552
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_020975.4(RET):c.1296A>G (p.Ala432=) rs1800860
NM_020975.5(RET):c.*1506G>A rs2742241
NM_020975.5(RET):c.-200A>G rs10900296

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.