ClinVar Miner

List of variants in gene SDHD studied for Hereditary Paraganglioma-Pheochromocytoma Syndromes

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 46
Download table as spreadsheet
HGVS dbSNP
NM_003002.3(SDHD):c.*(?_286)_*(387_?)del
NM_003002.3:c.1_169del
NM_003002.4(SDHD):c.*111A>G
NM_003002.4(SDHD):c.*302A>G rs201163059
NM_003002.4(SDHD):c.*428A>G rs184654032
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.112C>T (p.Arg38Ter) rs80338843
NM_003002.4(SDHD):c.118A>C (p.Ile40Leu) rs146276662
NM_003002.4(SDHD):c.136G>A (p.Val46Met) rs886047699
NM_003002.4(SDHD):c.148C>G (p.His50Asp) rs779249550
NM_003002.4(SDHD):c.170-1G>T rs1306475361
NM_003002.4(SDHD):c.174C>T (p.Gly58=)
NM_003002.4(SDHD):c.209G>A (p.Arg70Lys) rs755047928
NM_003002.4(SDHD):c.228C>T (p.Leu76=) rs148634289
NM_003002.4(SDHD):c.239T>G (p.Leu80Arg) rs1555187010
NM_003002.4(SDHD):c.242C>T (p.Pro81Leu) rs80338844
NM_003002.4(SDHD):c.267_281del (p.Ala90_Ser94del)
NM_003002.4(SDHD):c.274G>T (p.Asp92Tyr) rs80338845
NM_003002.4(SDHD):c.281C>G (p.Ser94Cys) rs199754684
NM_003002.4(SDHD):c.284T>C (p.Leu95Pro) rs80338846
NM_003002.4(SDHD):c.298_301del (p.Thr100fs) rs786203067
NM_003002.4(SDHD):c.314+1G>A rs1555187083
NM_003002.4(SDHD):c.315_480del (p.Trp105fs) rs1555187570
NM_003002.4(SDHD):c.328_330GTT[1] (p.Val111del) rs1555187580
NM_003002.4(SDHD):c.341A>G (p.Tyr114Cys) rs104894304
NM_003002.4(SDHD):c.342T>A (p.Tyr114Ter) rs1050032491
NM_003002.4(SDHD):c.381del (p.Leu128fs) rs1555187601
NM_003002.4(SDHD):c.3G>C (p.Met1Ile) rs80338842
NM_003002.4(SDHD):c.416T>C (p.Leu139Pro) rs80338847
NM_003002.4(SDHD):c.443G>T (p.Gly148Val) rs1555187633
NM_003002.4(SDHD):c.445A>G (p.Ile149Val)
NM_003002.4(SDHD):c.479G>T (p.Ter160Leu) rs201372601
NM_003002.4(SDHD):c.53-6C>A
NM_003002.4(SDHD):c.53C>T (p.Ala18Val) rs192332761
NM_003002.4(SDHD):c.53dup (p.Leu19fs) rs886041237
NM_003002.4(SDHD):c.57del (p.Leu20fs) rs587776649
NM_003002.4(SDHD):c.80G>A (p.Arg27Lys) rs200671534
NM_003002.4(SDHD):c.95C>A (p.Ser32Ter) rs104894305

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.