"PreventionGenetics, part of Exact Sciences"[submitter] AND "IL2RB"[ge - ClinVar - NCBI

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Items: 18

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1579140	NM_000878.5(IL2RB):c.1405C>T (p.Pro469Ser)	IL2RB (P469S)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 730177	NM_000878.5(IL2RB):c.1404C>T (p.Asp468=)	IL2RB	Single nucleotide variant (synonymous variant)	IL2RB-related disorder +1 more	GBenign
Select item 791374	NM_000878.5(IL2RB):c.1309G>A (p.Gly437Ser)	IL2RB (G437S)	Single nucleotide variant (missense variant)	IL2RB-related disorder +1 more	GBenign
Select item 1164671	NM_000878.5(IL2RB):c.1173C>A (p.Asp391Glu)	IL2RB (D391E)	Single nucleotide variant (missense variant)	not specified +2 more	GBenign
Select item 727903	NM_000878.5(IL2RB):c.960T>G (p.Pro320=)	IL2RB	Single nucleotide variant (synonymous variant)	IL2RB-related disorder +1 more	GLikely benign
Select item 711744	NM_000878.5(IL2RB):c.948C>T (p.Gly316=)	IL2RB	Single nucleotide variant (synonymous variant)	IL2RB-related disorder +1 more	GLikely benign
Select item 783886	NM_000878.5(IL2RB):c.811G>A (p.Gly271Arg)	IL2RB (G271R)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 1170851	NM_000878.5(IL2RB):c.750C>T (p.Gly250=)	IL2RB	Single nucleotide variant (synonymous variant)	not provided +3 more	GBenign
Select item 1461500	NM_000878.5(IL2RB):c.590C>T (p.Thr197Met)	IL2RB (T197M)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1165221	NM_000878.5(IL2RB):c.538-8C>T	IL2RB	Single nucleotide variant (intron variant)	Immunodeficiency 63 with lymphoproliferation and autoimmunity +2 more	GBenign
Select item 1008447	NM_000878.5(IL2RB):c.512C>T (p.Thr171Met)	IL2RB (T171M)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1645174	NM_000878.5(IL2RB):c.459A>C (p.Glu153Asp)	IL2RB (E153D)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 781528	NM_000878.5(IL2RB):c.248C>T (p.Ser83Phe)	IL2RB (S83F)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 719309	NM_000878.5(IL2RB):c.235G>A (p.Val79Met)	IL2RB (V79M)	Single nucleotide variant (missense variant)	IL2RB-related disorder +1 more	GBenign/Likely benign
Select item 1078584	NM_000878.5(IL2RB):c.234C>T (p.Pro78=)	IL2RB	Single nucleotide variant (synonymous variant)	IL2RB-related disorder +1 more	GLikely benign
Select item 871832	NM_000878.5(IL2RB):c.126C>T (p.Ala42=)	IL2RB	Single nucleotide variant (synonymous variant)	IL2RB-related disorder +1 more	GBenign/Likely benign
Select item 780653	NM_000878.5(IL2RB):c.120G>A (p.Ser40=)	IL2RB	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 1170852	NM_000878.5(IL2RB):c.88+3G>A	IL2RB	Single nucleotide variant (intron variant)	not provided +1 more	GBenign