List of variants in gene RAG1 reported as pathogenic for lymphoid system disorder

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_000448.3(RAG1):c.256_257del (p.Lys86fs)	rs772962160	0.00005
NM_000448.3(RAG1):c.1186C>T (p.Arg396Cys)	rs104894289	0.00002
NM_000448.3(RAG1):c.1682G>A (p.Arg561His)	rs104894284	0.00002
NM_000448.3(RAG1):c.2095C>T (p.Arg699Trp)	rs199474676	0.00002
NM_000448.3(RAG1):c.2210G>A (p.Arg737His)	rs104894286	0.00002
NM_000448.3(RAG1):c.1187G>A (p.Arg396His)	rs104894291	0.00001
NM_000448.3(RAG1):c.1421G>A (p.Arg474His)	rs199474686	0.00001
NM_000448.3(RAG1):c.1681C>T (p.Arg561Cys)	rs104894285	0.00001
NM_000448.3(RAG1):c.983G>A (p.Cys328Tyr)	rs121918571	0.00001
NM_000448.3(RAG1):c.1286A>G (p.Asp429Gly)	rs104894292
NM_000448.3(RAG1):c.1612_1624del (p.Ile538fs)	rs749256215
NM_000448.3(RAG1):c.2735A>G (p.Tyr912Cys)	rs104894290
NM_000448.3(RAG1):c.519del (p.Glu174fs)	rs1241698978
NM_000448.3(RAG1):c.775del (p.Ser259fs)	rs878853031

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