ClinVar Miner

List of variants in gene PRMT7 reported as pathogenic for developmental disorder of mental health

Included ClinVar conditions (728):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 13
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HGVS dbSNP gnomAD frequency
NM_019023.5(PRMT7):c.1056-1G>T rs201824659 0.00008
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.1480T>C (p.Trp494Arg) rs751670999 0.00001
NC_000016.9:g.68345747_68361056del
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.431_432del (p.Glu144fs) rs1567690011
NM_019023.5(PRMT7):c.622del (p.Gln208fs) rs2151732301
NM_019023.5(PRMT7):c.967C>T (p.Gln323Ter)
NM_019023.5(PRMT7):c.98C>A (p.Ser33Ter) rs2151436426

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