ClinVar Miner

List of variants in gene SETD2 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 35
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_014159.7(SETD2):c.5271C>T (p.Leu1757=) rs144825663 0.00389
NM_014159.7(SETD2):c.2783C>G (p.Thr928Arg) rs72895708 0.00228
NM_014159.7(SETD2):c.3567C>T (p.Thr1189=) rs140803915 0.00131
NM_014159.7(SETD2):c.3422C>T (p.Pro1141Leu) rs142723093 0.00088
NM_014159.7(SETD2):c.1885A>G (p.Lys629Glu) rs145650484 0.00047
NM_014159.7(SETD2):c.7164C>T (p.Thr2388=) rs144752494 0.00047
NM_014159.7(SETD2):c.7500C>T (p.Thr2500=) rs148499835 0.00036
NM_014159.7(SETD2):c.4193T>C (p.Ile1398Thr) rs145732065 0.00032
NM_014159.7(SETD2):c.6786C>T (p.Pro2262=) rs149552397 0.00032
NM_014159.7(SETD2):c.1986A>G (p.Gln662=) rs146562413 0.00026
NM_014159.7(SETD2):c.6455A>G (p.Tyr2152Cys) rs139628048 0.00024
NM_014159.7(SETD2):c.2096A>G (p.Asp699Gly) rs368132877 0.00022
NM_014159.7(SETD2):c.1412G>A (p.Arg471Lys) rs191313431 0.00021
NM_014159.7(SETD2):c.7350+6T>C rs369951554 0.00015
NM_014159.7(SETD2):c.265C>T (p.Leu89Phe) rs374799616 0.00014
NM_014159.7(SETD2):c.558G>A (p.Pro186=) rs183095591 0.00012
NM_014159.7(SETD2):c.2798G>T (p.Gly933Val) rs202209141 0.00010
NM_014159.7(SETD2):c.2849G>A (p.Arg950His) rs149265978 0.00004
NM_014159.7(SETD2):c.1914C>T (p.Ser638=) rs1371836213 0.00003
NM_014159.7(SETD2):c.475A>G (p.Thr159Ala) rs369333306 0.00003
NM_014159.7(SETD2):c.7239-8C>T rs375557161 0.00002
NM_014159.7(SETD2):c.3316T>C (p.Leu1106=) rs779666460 0.00001
NM_014159.7(SETD2):c.4680A>G (p.Lys1560=) rs780684040 0.00001
NM_014159.7(SETD2):c.2205C>G (p.Thr735=) rs1398507583
NM_014159.7(SETD2):c.2871A>G (p.Lys957=)
NM_014159.7(SETD2):c.3441G>A (p.Gln1147=)
NM_014159.7(SETD2):c.3458T>C (p.Ile1153Thr)
NM_014159.7(SETD2):c.4137C>T (p.Asp1379=) rs769080716
NM_014159.7(SETD2):c.4200T>C (p.Asp1400=)
NM_014159.7(SETD2):c.4332G>A (p.Leu1444=)
NM_014159.7(SETD2):c.5322T>C (p.His1774=)
NM_014159.7(SETD2):c.5574T>C (p.Pro1858=)
NM_014159.7(SETD2):c.5872G>C (p.Ala1958Pro) rs377115716
NM_014159.7(SETD2):c.772A>G (p.Thr258Ala)
NM_014159.7(SETD2):c.985C>A (p.Arg329=) rs372869995

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.