ClinVar Miner

List of variants in gene SLC25A22 reported as likely benign for not provided

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Total variants: 58
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HGVS dbSNP gnomAD frequency
NM_001191061.2(SLC25A22):c.-163-833G>T rs112748847 0.01178
NM_001191061.2(SLC25A22):c.-163-722C>T rs148671417 0.01093
NM_001191061.2(SLC25A22):c.146+22G>A rs114134153 0.00823
NM_001191061.2(SLC25A22):c.294-80G>A rs116352574 0.00738
NM_001191061.2(SLC25A22):c.-163-211del rs56900465 0.00642
NM_001191061.2(SLC25A22):c.*107G>A rs4963152 0.00380
NM_001191061.2(SLC25A22):c.-163-202G>T rs1301729368 0.00353
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.151G>A (p.Asp51Asn) rs116134953 0.00210
NM_001191061.2(SLC25A22):c.169G>A (p.Val57Ile) rs150242281 0.00204
NM_001191061.2(SLC25A22):c.412+38C>T rs200200466 0.00180
NM_001191061.2(SLC25A22):c.570C>T (p.Leu190=) rs145322467 0.00137
NM_001191061.2(SLC25A22):c.585C>T (p.Leu195=) rs147840220 0.00103
NM_001191061.2(SLC25A22):c.132C>T (p.Arg44=) rs146402942 0.00096
NM_001191061.2(SLC25A22):c.140C>T (p.Thr47Met) rs142220309 0.00068
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.413-8G>C rs376015598 0.00032
NM_001191061.2(SLC25A22):c.51C>T (p.Ile17=) rs566076909 0.00025
NM_001191061.2(SLC25A22):c.202+51G>A rs539960445 0.00024
NM_001191061.2(SLC25A22):c.679G>A (p.Val227Met) rs200603610 0.00024
NM_001191061.2(SLC25A22):c.678C>T (p.Tyr226=) rs200072903 0.00015
NM_001191061.2(SLC25A22):c.834C>T (p.His278=) rs187824231 0.00011
NM_001191061.2(SLC25A22):c.414C>T (p.Ala138=) rs199887745 0.00010
NM_001191061.2(SLC25A22):c.150C>T (p.Ser50=) rs201574228 0.00007
NM_001191061.2(SLC25A22):c.293+6G>A rs375955950 0.00007
NM_001191061.2(SLC25A22):c.146+11C>T rs372685549 0.00006
NM_001191061.2(SLC25A22):c.207T>G (p.Ala69=) rs527440140 0.00006
NM_001191061.2(SLC25A22):c.777C>T (p.Gly259=) rs373332611 0.00006
NM_001191061.2(SLC25A22):c.636C>T (p.Asn212=) rs760280356 0.00004
NM_001191061.2(SLC25A22):c.717C>T (p.Ala239=) rs545592967 0.00004
NM_001191061.2(SLC25A22):c.726C>T (p.Ala242=) rs771026197 0.00004
NM_001191061.2(SLC25A22):c.885C>T (p.Ile295=) rs543285265 0.00004
NM_001191061.2(SLC25A22):c.888G>A (p.Ala296=) rs768252518 0.00004
NM_001191061.2(SLC25A22):c.45C>T (p.Gly15=) rs748378875 0.00003
NM_001191061.2(SLC25A22):c.522C>T (p.Thr174=) rs772259110 0.00003
NM_001191061.2(SLC25A22):c.525C>T (p.Arg175=) rs368124957 0.00003
NM_001191061.2(SLC25A22):c.922C>T (p.Leu308=) rs758596118 0.00003
NM_001191061.2(SLC25A22):c.294-10C>T rs751196462 0.00002
NM_001191061.2(SLC25A22):c.657C>T (p.Ser219=) rs200830331 0.00002
NM_001191061.2(SLC25A22):c.818+15C>T rs201177114 0.00002
NM_001191061.2(SLC25A22):c.849C>T (p.Ala283=) rs1429166947 0.00002
NM_001191061.2(SLC25A22):c.141G>C (p.Thr47=) rs781681487 0.00001
NM_001191061.2(SLC25A22):c.147-11C>T rs748509400 0.00001
NM_001191061.2(SLC25A22):c.379C>T (p.Leu127=) rs746201051 0.00001
NM_001191061.2(SLC25A22):c.945G>A (p.Leu315=) rs1179494187 0.00001
NM_001191061.2(SLC25A22):c.-163-198A>T rs909242421
NM_001191061.2(SLC25A22):c.-163-199del rs1361777569
NM_001191061.2(SLC25A22):c.-163-206A>G rs57212291
NM_001191061.2(SLC25A22):c.-163-211T>A rs116665464
NM_001191061.2(SLC25A22):c.-72TCCACC[4] rs145401722
NM_001191061.2(SLC25A22):c.141G>A (p.Thr47=) rs781681487
NM_001191061.2(SLC25A22):c.327G>C (p.Ala109=) rs141975755
NM_001191061.2(SLC25A22):c.552C>A (p.Ala184=) rs368807589
NM_001191061.2(SLC25A22):c.666G>A (p.Lys222=) rs886048695
NM_001191061.2(SLC25A22):c.732C>T (p.Asn244=)

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