ClinVar Miner

List of variants in gene S1PR3

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Total variants: 35
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HGVS dbSNP gnomAD frequency
NM_005226.4(S1PR3):c.961C>T (p.Arg321Trp) rs199816019 0.00010
NM_005226.4(S1PR3):c.1079C>T (p.Pro360Leu) rs145641692 0.00006
NM_005226.4(S1PR3):c.896C>T (p.Thr299Met) rs768573223 0.00006
NM_005226.4(S1PR3):c.439G>A (p.Asp147Asn) rs755867055 0.00004
NM_005226.4(S1PR3):c.919C>T (p.Arg307Trp) rs142147868 0.00004
NM_005226.4(S1PR3):c.141G>C (p.Leu47Phe) rs202246737 0.00002
NM_005226.4(S1PR3):c.704C>T (p.Ser235Leu) rs376050822 0.00002
NM_005226.4(S1PR3):c.1085C>T (p.Ser362Phe) rs778116595 0.00001
NM_005226.4(S1PR3):c.1098C>A (p.Asp366Glu) rs1825879718 0.00001
NM_005226.4(S1PR3):c.590T>C (p.Ile197Thr) rs937311956 0.00001
NM_005226.4(S1PR3):c.692A>G (p.Asn231Ser) rs1391725932 0.00001
NM_005226.4(S1PR3):c.874G>A (p.Ala292Thr) rs376947296 0.00001
NM_005226.4(S1PR3):c.1046C>A (p.Pro349Gln) rs373695744
NM_005226.4(S1PR3):c.1093A>C (p.Met365Leu) rs376847603
NM_005226.4(S1PR3):c.1093A>G (p.Met365Val) rs376847603
NM_005226.4(S1PR3):c.1097A>G (p.Asp366Gly)
NM_005226.4(S1PR3):c.23G>A (p.Arg8His)
NM_005226.4(S1PR3):c.32C>T (p.Pro11Leu)
NM_005226.4(S1PR3):c.38G>C (p.Arg13Pro) rs201961912
NM_005226.4(S1PR3):c.407G>A (p.Arg136Gln)
NM_005226.4(S1PR3):c.446A>G (p.Asn149Ser) rs2547342691
NM_005226.4(S1PR3):c.457C>T (p.Arg153Cys)
NM_005226.4(S1PR3):c.480G>T (p.Met160Ile) rs2547342719
NM_005226.4(S1PR3):c.538C>T (p.His180Tyr)
NM_005226.4(S1PR3):c.587A>T (p.Tyr196Phe) rs909885163
NM_005226.4(S1PR3):c.652A>G (p.Ile218Val)
NM_005226.4(S1PR3):c.679C>T (p.Arg227Cys)
NM_005226.4(S1PR3):c.709C>T (p.Arg237Trp)
NM_005226.4(S1PR3):c.760G>A (p.Ala254Thr)
NM_005226.4(S1PR3):c.806G>A (p.Cys269Tyr)
NM_005226.4(S1PR3):c.931C>G (p.Arg311Gly) rs753129196
NM_005226.4(S1PR3):c.962G>C (p.Arg321Pro) rs138065168
NM_005226.4(S1PR3):c.964G>A (p.Gly322Arg)
NM_005226.4(S1PR3):c.989C>T (p.Pro330Leu)
NM_005226.4(S1PR3):c.997G>T (p.Asp333Tyr) rs758690327

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