List of variants in gene RNF13 studied for Developmental and epileptic encephalopathy, 73

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_183381.3(RNF13):c.789C>T (p.His263=)	rs6768054	0.63113
NM_183381.3(RNF13):c.1045A>G (p.Thr349Ala)	rs972002974	0.00001
NM_183381.3(RNF13):c.613A>G (p.Lys205Glu)	rs771241791	0.00001
NM_183381.3(RNF13):c.106A>G (p.Ile36Val)
NM_183381.3(RNF13):c.262A>T (p.Asn88Tyr)
NM_183381.3(RNF13):c.651A>T (p.Arg217Ser)
NM_183381.3(RNF13):c.881_882del (p.Asp293_Ser294insTer)	rs2108622234
NM_183381.3(RNF13):c.898C>T (p.Gln300Ter)	rs1435275372
NM_183381.3(RNF13):c.901G>T (p.Glu301Ter)
NM_183381.3(RNF13):c.919G>T (p.Glu307Ter)
NM_183381.3(RNF13):c.929del (p.Pro310fs)
NM_183381.3(RNF13):c.932T>C (p.Leu311Ser)	rs1559980771
NM_183381.3(RNF13):c.935T>C (p.Leu312Pro)	rs1559980785
NM_183381.3(RNF13):c.950_951del (p.Ser317fs)	rs2108622490

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