Related gene-specific medical variations for Gene (Select 3565) - ClinVar - NCBI

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Links from Gene

Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3109426	NM_000589.4(IL4):c.425C>T (p.Thr142Met)	IL4, LOC105379176 (T126M +1 more)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 3109425	NM_000589.4(IL4):c.349C>G (p.Leu117Val)	IL4, LOC105379176 (L101V +1 more)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 3109424	NM_000589.4(IL4):c.263G>A (p.Arg88His)	IL4, LOC105379176 (R72H +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2490569	NM_000589.4(IL4):c.301A>C (p.Lys101Gln)	IL4, LOC105379176 (K101Q +1 more)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 2478049	NM_000589.4(IL4):c.323A>C (p.Lys108Thr)	IL4, LOC105379176 (K108T +1 more)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 2213538	NM_000589.4(IL4):c.331G>A (p.Asp111Asn)	IL4, LOC105379176 (D95N +1 more)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 2211668	NM_000589.4(IL4):c.290T>C (p.Phe97Ser)	IL4, LOC105379176 (F97S +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2205307	NM_000589.4(IL4):c.218C>T (p.Ala73Val)	IL4, LOC105379176 (A57V +2 more)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 782744	NM_000589.4(IL4):c.333C>T (p.Asp111=)	IL4, LOC105379176	Single nucleotide variant (non-coding transcript variant +2 more)	not provided	GBenign