ClinVar Miner

List of variants in gene SLC25A22 reported as benign by Invitae

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Gene type:
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Total variants: 16
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HGVS dbSNP gnomAD frequency
NM_001191061.2(SLC25A22):c.234C>T (p.Pro78=) rs80335370 0.09454
NM_001191061.2(SLC25A22):c.448C>G (p.Leu150Val) rs111277421 0.06224
NM_001191061.2(SLC25A22):c.561C>T (p.Tyr187=) rs77117049 0.03987
NM_001191061.2(SLC25A22):c.412+10G>T rs113091974 0.03661
NM_001191061.2(SLC25A22):c.705T>C (p.Ala235=) rs142861804 0.00262
NM_001191061.2(SLC25A22):c.500G>A (p.Arg167Gln) rs201089795 0.00248
NM_001191061.2(SLC25A22):c.169G>A (p.Val57Ile) rs150242281 0.00204
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 0.00103
NM_001191061.2(SLC25A22):c.495C>T (p.Ala165=) rs374780430 0.00063
NM_001191061.2(SLC25A22):c.294-13G>A rs201472482 0.00030
NM_001191061.2(SLC25A22):c.743-16C>T rs200493024 0.00007
NM_001191061.2(SLC25A22):c.20+18dup rs796053236
NM_001191061.2(SLC25A22):c.203-11del
NM_001191061.2(SLC25A22):c.742+19G>A rs373084007

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