ClinVar Miner

List of variants in gene SLC25A22 reported as benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 46
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001191061.2(SLC25A22):c.-163-197C>T rs28501311 0.95686
NM_001191061.2(SLC25A22):c.-163-206del rs138179760 0.86902
NM_001191061.2(SLC25A22):c.234C>T (p.Pro78=) rs80335370 0.09426
NM_001191061.2(SLC25A22):c.293+27G>A rs79478359 0.08883
NM_001191061.2(SLC25A22):c.448C>G (p.Leu150Val) rs111277421 0.06224
NM_001191061.2(SLC25A22):c.-163-868T>C rs111520133 0.05673
NM_001191061.2(SLC25A22):c.561C>T (p.Tyr187=) rs77117049 0.03719
NM_001191061.2(SLC25A22):c.412+10G>T rs113091974 0.03661
NM_001191061.2(SLC25A22):c.-164+847A>G rs114582611 0.03049
NM_001191061.2(SLC25A22):c.-163-881C>T rs115490180 0.02548
NM_001191061.2(SLC25A22):c.413-36G>C rs138578986 0.02006
NM_001191061.2(SLC25A22):c.147-128G>A rs74045130 0.01909
NM_001191061.2(SLC25A22):c.147-22C>T rs114424122 0.01887
NM_001191061.2(SLC25A22):c.705T>C (p.Ala235=) rs142861804 0.00238
NM_001191061.2(SLC25A22):c.169G>A (p.Val57Ile) rs150242281 0.00204
NM_001191061.2(SLC25A22):c.151G>A (p.Asp51Asn) rs116134953 0.00198
NM_001191061.2(SLC25A22):c.570C>T (p.Leu190=) rs145322467 0.00137
NM_001191061.2(SLC25A22):c.618G>A (p.Pro206=) rs150544061 0.00118
NM_001191061.2(SLC25A22):c.585C>T (p.Leu195=) rs147840220 0.00097
NM_001191061.2(SLC25A22):c.132C>T (p.Arg44=) rs146402942 0.00096
NM_001191061.2(SLC25A22):c.*17A>C rs554507285 0.00089
NM_001191061.2(SLC25A22):c.495C>T (p.Ala165=) rs374780430 0.00063
NM_001191061.2(SLC25A22):c.876G>A (p.Ala292=) rs146300431 0.00058
NM_001191061.2(SLC25A22):c.327G>A (p.Ala109=) rs141975755 0.00049
NM_001191061.2(SLC25A22):c.743-12C>T rs200517971 0.00041
NM_001191061.2(SLC25A22):c.413-8G>C rs376015598 0.00032
NM_001191061.2(SLC25A22):c.294-13G>A rs201472482 0.00030
NM_001191061.2(SLC25A22):c.-155T>C rs886048702 0.00013
NM_001191061.2(SLC25A22):c.414C>T (p.Ala138=) rs199887745 0.00011
NM_001191061.2(SLC25A22):c.897C>T (p.Phe299=) rs7124179 0.00011
NM_001191061.2(SLC25A22):c.-151G>A rs587781167 0.00009
NM_001191061.2(SLC25A22):c.579G>A (p.Thr193=) rs141430143 0.00009
NM_001191061.2(SLC25A22):c.413-12C>T rs587781169 0.00008
NM_001191061.2(SLC25A22):c.75C>T (p.Cys25=) rs764930724 0.00007
NM_001191061.2(SLC25A22):c.-41C>T rs376603464 0.00006
NM_001191061.2(SLC25A22):c.294-20C>T rs755464940 0.00005
NM_001191061.2(SLC25A22):c.819-16C>T rs572751087 0.00005
NM_001191061.2(SLC25A22):c.933G>A (p.Ala311=) rs587781170 0.00005
NM_001191061.2(SLC25A22):c.202+14C>T rs587781168 0.00004
NM_001191061.2(SLC25A22):c.21-15C>T rs759055009 0.00004
NM_001191061.2(SLC25A22):c.294-14C>T rs200362178 0.00003
NM_001191061.2(SLC25A22):c.-163-211T>G rs116665464
NM_001191061.2(SLC25A22):c.-163-262_-163-244dup rs568118950
NM_001191061.2(SLC25A22):c.-163-837G>T rs74045131
NM_001191061.2(SLC25A22):c.20+18dup rs796053236
NM_001191061.2(SLC25A22):c.742+19G>A rs373084007

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.