List of variants in gene combination BCL10, LOC126805771 reported as uncertain significance for Immunodeficiency 37

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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: 4

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HGVS	dbSNP	gnomAD frequency
NM_003921.5(BCL10):c.14C>G (p.Ala5Gly)	rs778423633	0.00001
NM_003921.5(BCL10):c.1A>T (p.Met1Leu)	rs2527119955
NM_003921.5(BCL10):c.20C>G (p.Ser7Cys)	rs1268648553
NM_003921.5(BCL10):c.28G>A (p.Glu10Lys)	rs1403156514

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