ClinVar Miner

List of variants in gene PRMT7 studied for developmental disorder of mental health

Included ClinVar conditions (728):
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Gene type:
ClinVar version:
Total variants: 44
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HGVS dbSNP gnomAD frequency
NM_019023.5(PRMT7):c.1797C>T (p.Thr599=) rs1131933 0.48912
NM_019023.5(PRMT7):c.1638C>T (p.Asp546=) rs61746794 0.13248
NM_019023.5(PRMT7):c.1276-18G>A rs7190134 0.13231
NM_019023.5(PRMT7):c.1905C>T (p.Pro635=) rs61733486 0.06161
NM_019023.5(PRMT7):c.1945G>A (p.Val649Ile) rs143131470 0.00022
NM_019023.5(PRMT7):c.1056-1G>T rs201824659 0.00008
NM_019023.5(PRMT7):c.499G>A (p.Val167Met) rs138763605 0.00007
NM_019023.5(PRMT7):c.1726G>A (p.Glu576Lys) rs377019678 0.00006
NM_019023.5(PRMT7):c.1490G>A (p.Arg497Gln) rs753756119 0.00004
NM_019023.5(PRMT7):c.1078C>T (p.Arg360Cys) rs775110866 0.00003
NM_019023.5(PRMT7):c.1489C>T (p.Arg497Trp) rs1201730206 0.00003
NM_019023.5(PRMT7):c.95G>C (p.Arg32Thr) rs149170494 0.00003
NM_019023.5(PRMT7):c.1159A>G (p.Arg387Gly) rs762515973 0.00001
NM_019023.5(PRMT7):c.1220G>A (p.Cys407Tyr) rs1313637057 0.00001
NM_019023.5(PRMT7):c.1323+2T>G rs1339009950 0.00001
NM_019023.5(PRMT7):c.1480T>C (p.Trp494Arg) rs751670999 0.00001
NM_019023.5(PRMT7):c.454G>A (p.Gly152Arg) rs200195216 0.00001
NM_019023.5(PRMT7):c.455G>A (p.Gly152Glu) rs369694211 0.00001
NM_019023.5(PRMT7):c.820C>T (p.Arg274Ter) rs372375423 0.00001
NC_000016.9:g.68345747_68361056del
NM_019023.5(PRMT7):c.-218-3C>G
NM_019023.5(PRMT7):c.1074_1075del (p.Arg358fs) rs763953657
NM_019023.5(PRMT7):c.1097G>A (p.Cys366Tyr) rs2151827144
NM_019023.5(PRMT7):c.1239_1246dup (p.Val416fs) rs1567721991
NM_019023.5(PRMT7):c.1276-1G>A rs886039897
NM_019023.5(PRMT7):c.1335_1338dup (p.His447Ter)
NM_019023.5(PRMT7):c.1499dup (p.Asp501fs) rs1567739042
NM_019023.5(PRMT7):c.1650+27A>C rs1868159
NM_019023.5(PRMT7):c.1651-8G>A
NM_019023.5(PRMT7):c.1652G>A (p.Arg551His)
NM_019023.5(PRMT7):c.1915T>C (p.Cys639Arg)
NM_019023.5(PRMT7):c.1949A>G (p.Tyr650Cys) rs1033540334
NM_019023.5(PRMT7):c.2029G>A (p.Asp677Asn)
NM_019023.5(PRMT7):c.254C>A (p.Ala85Glu)
NM_019023.5(PRMT7):c.282+3A>G rs2082913032
NM_019023.5(PRMT7):c.322G>T (p.Glu108Ter) rs1014959895
NM_019023.5(PRMT7):c.347T>A (p.Ile116Asn) rs2151558358
NM_019023.5(PRMT7):c.431_432del (p.Glu144fs) rs1567690011
NM_019023.5(PRMT7):c.457dup (p.Glu153fs) rs2151701931
NM_019023.5(PRMT7):c.542A>G (p.Tyr181Cys)
NM_019023.5(PRMT7):c.622del (p.Gln208fs) rs2151732301
NM_019023.5(PRMT7):c.927G>T (p.Gln309His) rs1597361540
NM_019023.5(PRMT7):c.967C>T (p.Gln323Ter)
NM_019023.5(PRMT7):c.98C>A (p.Ser33Ter) rs2151436426

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