List of variants in gene IL2RB reported by CeGaT Center for Human Genetics Tuebingen

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: 16

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HGVS	dbSNP	gnomAD frequency
NM_000878.5(IL2RB):c.235G>A (p.Val79Met)	rs149508414	0.00319
NM_000878.5(IL2RB):c.810C>T (p.Thr270=)	rs115475423	0.00223
NM_000878.5(IL2RB):c.126C>T (p.Ala42=)	rs148800183	0.00116
NM_000878.5(IL2RB):c.949G>A (p.Gly317Ser)	rs143857582	0.00103
NM_000878.5(IL2RB):c.1152C>T (p.Tyr384=)	rs146986731	0.00073
NM_000878.5(IL2RB):c.234C>T (p.Pro78=)	rs111730897	0.00040
NM_000878.5(IL2RB):c.1001C>T (p.Thr334Met)	rs146173891	0.00021
NM_000878.5(IL2RB):c.538-3C>T	rs748309662	0.00002
NM_000878.5(IL2RB):c.1257C>T (p.Cys419=)	rs779196758	0.00001
NM_000878.5(IL2RB):c.663C>T (p.Ser221=)	rs781721809	0.00001
NM_000878.5(IL2RB):c.1140G>T (p.Val380=)	rs775624588
NM_000878.5(IL2RB):c.1305C>G (p.Leu435=)	rs768964296
NM_000878.5(IL2RB):c.1467T>G (p.Pro489=)
NM_000878.5(IL2RB):c.388+1G>A	rs747978443
NM_000878.5(IL2RB):c.598C>T (p.Pro200Ser)	rs1921696300
NM_000878.5(IL2RB):c.921C>T (p.Pro307=)

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