ClinVar Miner

List of variants in gene SLC10A2 reported as benign for not provided

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Total variants: 21
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HGVS dbSNP gnomAD frequency
NM_000452.3(SLC10A2):c.511T>G (p.Ser171Ala) rs188096 0.88630
NM_000452.3(SLC10A2):c.920-20G>A rs279940 0.88488
NM_000452.3(SLC10A2):c.761+28A>G rs8000956 0.44539
NM_000452.3(SLC10A2):c.292G>A (p.Val98Ile) rs55971546 0.02814
NM_000452.3(SLC10A2):c.505C>T (p.Leu169=) rs41281678 0.02689
NM_000452.3(SLC10A2):c.868C>T (p.Pro290Ser) rs56398830 0.00998
NM_000452.3(SLC10A2):c.886T>C (p.Phe296Leu) rs71640248 0.00537
NM_000452.3(SLC10A2):c.516C>T (p.Leu172=) rs114146899 0.00201
NM_000452.3(SLC10A2):c.66T>C (p.Pro22=) rs138387807 0.00112
NM_000452.3(SLC10A2):c.1038C>T (p.Asp346=) rs147498129 0.00094
NM_000452.3(SLC10A2):c.80A>G (p.Asn27Ser) rs147075283 0.00046
NM_000452.3(SLC10A2):c.190C>T (p.Arg64Trp) rs142620512 0.00002
NM_000452.2(SLC10A2):c.586-4dup rs199940758
NM_000452.3(SLC10A2):c.129C>T (p.Ala43=)
NM_000452.3(SLC10A2):c.156C>T (p.Asn52=)
NM_000452.3(SLC10A2):c.377+12T>C
NM_000452.3(SLC10A2):c.378-12A>G
NM_000452.3(SLC10A2):c.426G>A (p.Pro142=) rs157381
NM_000452.3(SLC10A2):c.475G>A (p.Val159Ile)
NM_000452.3(SLC10A2):c.511= (p.Ser171=)
NM_000452.3(SLC10A2):c.586-4del

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