IL7[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2512658	NM_000880.4(IL7):c.514A>G (p.Met172Val)	IL7 (M110V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3109465	NM_000880.4(IL7):c.383C>T (p.Ala128Val)	IL7 (A128V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2479097	NM_000880.4(IL7):c.364A>G (p.Lys122Glu)	IL7 (K78E +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3042451	NM_000880.4(IL7):c.360+6C>T	IL7	Single nucleotide variant (intron variant)	IL7-related disorder	GBenign
Select item 2620502	NM_000880.4(IL7):c.356G>A (p.Gly119Asp)	IL7 (G119D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3285908	NM_000880.4(IL7):c.341T>A (p.Leu114Gln)	IL7 (L114Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 694068	NM_000880.4(IL7):c.205A>T (p.Arg69Ter)	IL7 (R69*)	Single nucleotide variant (nonsense)	Epidermodysplasia verruciformis, susceptibility to, 5	Grisk factor
Select item 2319294	NM_000880.4(IL7):c.155T>C (p.Met52Thr)	IL7 (M52T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2688314	NM_000880.4(IL7):c.148-6865A>T	IL7	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 750372	NM_000880.4(IL7):c.111T>C (p.Tyr37=)	IL7	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3043304	NM_000880.4(IL7):c.52G>A (p.Val18Ile)	IL7 (V18I)	Single nucleotide variant (missense variant)	IL7-related disorder	GBenign
Select item 728954	NM_000880.4(IL7):c.10+7G>A	IL7	Single nucleotide variant (intron variant)	not provided	GBenign