ClinVar Miner

List of variants in gene S1PR2 reported as uncertain significance for not provided

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Total variants: 38
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HGVS dbSNP gnomAD frequency
NM_004230.4(S1PR2):c.574C>T (p.Leu192=) rs548754912 0.00016
NM_004230.4(S1PR2):c.826G>A (p.Val276Ile) rs146537931 0.00013
NM_004230.4(S1PR2):c.71C>T (p.Thr24Met) rs189645503 0.00009
NM_004230.4(S1PR2):c.632G>A (p.Arg211His) rs141230424 0.00007
NM_004230.4(S1PR2):c.944G>A (p.Arg315Gln) rs777226501 0.00007
NM_004230.4(S1PR2):c.113C>G (p.Ala38Gly) rs776432035 0.00005
NM_004230.4(S1PR2):c.955G>A (p.Gly319Arg) rs139097585 0.00004
NM_004230.4(S1PR2):c.986G>A (p.Arg329His) rs143246348 0.00004
NM_004230.4(S1PR2):c.578G>T (p.Cys193Phe) rs780666522 0.00003
NM_004230.4(S1PR2):c.650G>A (p.Arg217His) rs138962414 0.00003
NM_004230.4(S1PR2):c.781G>A (p.Val261Ile) rs199824841 0.00003
NM_004230.4(S1PR2):c.107C>T (p.Ala36Val) rs747663144 0.00002
NM_004230.4(S1PR2):c.229G>A (p.Ala77Thr) rs750224099 0.00002
NM_004230.4(S1PR2):c.230C>T (p.Ala77Val) rs779058016 0.00001
NM_004230.4(S1PR2):c.388C>T (p.Arg130Cys) rs200439929 0.00001
NM_004230.4(S1PR2):c.664G>C (p.Asp222His) rs747191535 0.00001
NM_004230.4(S1PR2):c.877C>T (p.Arg293Trp) rs370698200 0.00001
NM_004230.4(S1PR2):c.889C>T (p.Arg297Trp) rs763068319 0.00001
NM_004230.4(S1PR2):c.934G>C (p.Val312Leu) rs750507202 0.00001
NM_004230.4(S1PR2):c.985C>T (p.Arg329Cys) rs765378016 0.00001
NM_004230.4(S1PR2):c.1013T>C (p.Met338Thr)
NM_004230.4(S1PR2):c.1034C>T (p.Thr345Met) rs540296894
NM_004230.4(S1PR2):c.136G>A (p.Ala46Thr)
NM_004230.4(S1PR2):c.203T>C (p.Met68Thr)
NM_004230.4(S1PR2):c.250G>A (p.Val84Met)
NM_004230.4(S1PR2):c.290C>T (p.Thr97Met) rs1431090035
NM_004230.4(S1PR2):c.341T>G (p.Ile114Ser) rs2513959841
NM_004230.4(S1PR2):c.344C>T (p.Thr115Met) rs979923055
NM_004230.4(S1PR2):c.352G>C (p.Ala118Pro)
NM_004230.4(S1PR2):c.407A>G (p.Lys136Arg) rs2513959737
NM_004230.4(S1PR2):c.424A>G (p.Ser142Gly) rs2145441223
NM_004230.4(S1PR2):c.429C>T (p.Asp143=) rs774990809
NM_004230.4(S1PR2):c.444G>C (p.Met148Ile) rs2039616917
NM_004230.4(S1PR2):c.643G>A (p.Val215Met)
NM_004230.4(S1PR2):c.677C>T (p.Pro226Leu)
NM_004230.4(S1PR2):c.794C>A (p.Pro265Gln) rs572711891
NM_004230.4(S1PR2):c.863A>G (p.Tyr288Cys) rs2513958866
NM_004230.4(S1PR2):c.995G>T (p.Ser332Ile)

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