ClinVar Miner

List of variants in gene LOC126861339, SDHD studied for adrenal gland neoplasm

Included ClinVar conditions (53):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 98
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HGVS dbSNP gnomAD frequency
NM_003002.4(SDHD):c.34G>A (p.Gly12Ser) rs34677591 0.00706
NM_003002.4(SDHD):c.38C>T (p.Ala13Val) rs750080041 0.00003
NM_003002.4(SDHD):c.52+13C>G rs954474648 0.00003
NM_003002.4(SDHD):c.18G>A (p.Arg6=) rs200895313 0.00002
NM_003002.4(SDHD):c.52+8G>A rs370761122 0.00002
NM_003002.4(SDHD):c.13T>C (p.Trp5Arg) rs778202647 0.00001
NM_003002.4(SDHD):c.1A>T (p.Met1Leu) rs104894307 0.00001
NM_003002.4(SDHD):c.21G>A (p.Leu7=) rs974401612 0.00001
NM_003002.4(SDHD):c.25G>T (p.Ala9Ser) rs772671893 0.00001
NM_003002.4(SDHD):c.33C>T (p.Cys11=) rs104894309 0.00001
NM_003002.4(SDHD):c.35G>A (p.Gly12Asp) rs764384503 0.00001
NM_003002.4(SDHD):c.49C>G (p.Arg17Gly) rs1314133983 0.00001
NM_003002.4(SDHD):c.52+19C>T rs1566690388 0.00001
NM_003002.4(SDHD):c.5C>T (p.Ala2Val) rs1440670464 0.00001
NC_000011.10:g.(?_112086898)_(112094980_?)del
NC_000011.9:g.(?_111957622)_(111965704_?)dup
NM_003002.3(SDHD):c.-84_*831del
NM_003002.4(SDHD):c.10C>A (p.Leu4Ile)
NM_003002.4(SDHD):c.10C>T (p.Leu4Phe) rs1032016970
NM_003002.4(SDHD):c.10dup (p.Leu4fs) rs878854589
NM_003002.4(SDHD):c.12C>T (p.Leu4=) rs2135264636
NM_003002.4(SDHD):c.13T>A (p.Trp5Arg)
NM_003002.4(SDHD):c.13_14del (p.Trp5fs) rs1566690018
NM_003002.4(SDHD):c.14G>A (p.Trp5Ter) rs104894310
NM_003002.4(SDHD):c.14_30del (p.Trp5fs)
NM_003002.4(SDHD):c.15G>A (p.Trp5Ter)
NM_003002.4(SDHD):c.16A>G (p.Arg6Gly) rs11547889
NM_003002.4(SDHD):c.17G>A (p.Arg6Lys)
NM_003002.4(SDHD):c.18G>T (p.Arg6Ser) rs200895313
NM_003002.4(SDHD):c.18_21del (p.Leu7fs) rs1555186662
NM_003002.4(SDHD):c.19C>T (p.Leu7=) rs1337542194
NM_003002.4(SDHD):c.1A>G (p.Met1Val) rs104894307
NM_003002.4(SDHD):c.20T>A (p.Leu7Gln) rs1865619523
NM_003002.4(SDHD):c.20T>C (p.Leu7Pro) rs1865619523
NM_003002.4(SDHD):c.20T>G (p.Leu7Arg) rs1865619523
NM_003002.4(SDHD):c.21G>T (p.Leu7=)
NM_003002.4(SDHD):c.22A>G (p.Ser8Gly) rs1865619629
NM_003002.4(SDHD):c.23G>A (p.Ser8Asn) rs558914063
NM_003002.4(SDHD):c.25G>A (p.Ala9Thr) rs772671893
NM_003002.4(SDHD):c.26C>G (p.Ala9Gly) rs1592777287
NM_003002.4(SDHD):c.26C>T (p.Ala9Val) rs1592777287
NM_003002.4(SDHD):c.27C>A (p.Ala9=) rs1555186670
NM_003002.4(SDHD):c.27C>G (p.Ala9=)
NM_003002.4(SDHD):c.27C>T (p.Ala9=) rs1555186670
NM_003002.4(SDHD):c.28G>A (p.Val10Ile) rs1555186671
NM_003002.4(SDHD):c.2T>C (p.Met1Thr)
NM_003002.4(SDHD):c.33C>A (p.Cys11Ter) rs104894309
NM_003002.4(SDHD):c.34G>C (p.Gly12Arg)
NM_003002.4(SDHD):c.35G>T (p.Gly12Val) rs764384503
NM_003002.4(SDHD):c.36T>G (p.Gly12=) rs1592777328
NM_003002.4(SDHD):c.37G>A (p.Ala13Thr) rs940936212
NM_003002.4(SDHD):c.37G>T (p.Ala13Ser) rs940936212
NM_003002.4(SDHD):c.38C>G (p.Ala13Gly) rs750080041
NM_003002.4(SDHD):c.39C>T (p.Ala13=) rs1566690237
NM_003002.4(SDHD):c.3G>A (p.Met1Ile) rs80338842
NM_003002.4(SDHD):c.3G>C (p.Met1Ile) rs80338842
NM_003002.4(SDHD):c.40C>T (p.Leu14=) rs1060503772
NM_003002.4(SDHD):c.42A>G (p.Leu14=) rs878854593
NM_003002.4(SDHD):c.42A>T (p.Leu14=)
NM_003002.4(SDHD):c.43G>C (p.Gly15Arg) rs1476121898
NM_003002.4(SDHD):c.44G>A (p.Gly15Glu)
NM_003002.4(SDHD):c.44G>C (p.Gly15Ala) rs1865621392
NM_003002.4(SDHD):c.44_52+24del rs1865621296
NM_003002.4(SDHD):c.45A>T (p.Gly15=) rs2135264801
NM_003002.4(SDHD):c.46G>C (p.Gly16Arg) rs1555186687
NM_003002.4(SDHD):c.46G>T (p.Gly16Cys) rs1555186687
NM_003002.4(SDHD):c.47G>A (p.Gly16Asp)
NM_003002.4(SDHD):c.47G>T (p.Gly16Val)
NM_003002.4(SDHD):c.48C>T (p.Gly16=) rs1555186688
NM_003002.4(SDHD):c.49C>T (p.Arg17Ter) rs1314133983
NM_003002.4(SDHD):c.4G>A (p.Ala2Thr) rs1401420432
NM_003002.4(SDHD):c.50G>A (p.Arg17Gln) rs1865621723
NM_003002.4(SDHD):c.51A>C (p.Arg17=) rs199890548
NM_003002.4(SDHD):c.52+10C>G rs2135264901
NM_003002.4(SDHD):c.52+11T>A
NM_003002.4(SDHD):c.52+12T>C rs1865622422
NM_003002.4(SDHD):c.52+13C>T
NM_003002.4(SDHD):c.52+15C>T rs1486681280
NM_003002.4(SDHD):c.52+17C>G
NM_003002.4(SDHD):c.52+17C>T rs2135264969
NM_003002.4(SDHD):c.52+18C>T
NM_003002.4(SDHD):c.52+1G>A rs1592777386
NM_003002.4(SDHD):c.52+1_52+2delinsAA
NM_003002.4(SDHD):c.52+20T>C
NM_003002.4(SDHD):c.52+2T>C rs587776644
NM_003002.4(SDHD):c.52+2T>G rs587776644
NM_003002.4(SDHD):c.52+5G>A rs1592777393
NM_003002.4(SDHD):c.52+5G>C rs1592777393
NM_003002.4(SDHD):c.52+6G>A rs1416678757
NM_003002.4(SDHD):c.52+7G>C rs2135264872
NM_003002.4(SDHD):c.52+8del rs2135264855
NM_003002.4(SDHD):c.52+8dup rs2135264855
NM_003002.4(SDHD):c.5C>G (p.Ala2Gly) rs1440670464
NM_003002.4(SDHD):c.6G>A (p.Ala2=) rs1592777160
NM_003002.4(SDHD):c.7G>A (p.Val3Ile) rs1555186656
NM_003002.4(SDHD):c.7G>C (p.Val3Leu) rs1555186656
NM_003002.4(SDHD):c.7G>T (p.Val3Phe) rs1555186656
NM_003002.4(SDHD):c.9T>A (p.Val3=) rs1555186657

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