ClinVar Miner

List of variants in gene combination LOC130009747, SUCLA2

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Total variants: 28
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HGVS dbSNP gnomAD frequency
NM_003850.3(SUCLA2):c.90+24G>A rs9567972 0.71583
NM_003850.3(SUCLA2):c.90+76G>C rs7982426 0.06060
NM_003850.3(SUCLA2):c.45C>T (p.Thr15=) rs35899901 0.00624
NM_003850.3(SUCLA2):c.37G>A (p.Val13Met) rs35201084 0.00371
NM_003850.3(SUCLA2):c.49C>G (p.Arg17Gly) rs200124902 0.00024
NM_003850.3(SUCLA2):c.88C>G (p.Gln30Glu) rs568437392 0.00008
NM_003850.3(SUCLA2):c.78G>A (p.Arg26=) rs1174121047 0.00005
NM_003850.3(SUCLA2):c.36C>G (p.Ala12=) rs771793708 0.00004
NM_003850.3(SUCLA2):c.80C>T (p.Ala27Val) rs368407554 0.00003
NM_003850.3(SUCLA2):c.90+19C>T rs370867973 0.00003
NM_003850.3(SUCLA2):c.90+6G>A rs1051697976 0.00003
NM_003850.3(SUCLA2):c.58C>T (p.Arg20Trp) rs757550710 0.00001
NM_003850.3(SUCLA2):c.64C>T (p.Arg22Trp) rs752527887 0.00001
NM_003850.3(SUCLA2):c.90+14del rs1278242539 0.00001
NM_003850.3(SUCLA2):c.35C>T (p.Ala12Val) rs1247189411
NM_003850.3(SUCLA2):c.36C>T (p.Ala12=) rs771793708
NM_003850.3(SUCLA2):c.39G>A (p.Val13=) rs894388833
NM_003850.3(SUCLA2):c.46C>G (p.Leu16Val)
NM_003850.3(SUCLA2):c.54C>A (p.Asn18Lys) rs2541720907
NM_003850.3(SUCLA2):c.54C>T (p.Asn18=)
NM_003850.3(SUCLA2):c.68C>G (p.Thr23Arg) rs538760468
NM_003850.3(SUCLA2):c.68C>T (p.Thr23Met) rs538760468
NM_003850.3(SUCLA2):c.69G>A (p.Thr23=) rs1324777274
NM_003850.3(SUCLA2):c.77G>A (p.Arg26Gln) rs2541720846
NM_003850.3(SUCLA2):c.81T>G (p.Ala27=) rs1411239127
NM_003850.3(SUCLA2):c.86C>A (p.Ala29Asp) rs1182235529
NM_003850.3(SUCLA2):c.90+17C>T rs773993642
NM_003850.3(SUCLA2):c.90+7C>A rs771607199

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