C3151405[trait identifier] AND "Illumina Laboratory Services, Illumina - ClinVar - NCBI

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Items: 18

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 357463	NM_052872.4(IL17F):c.*243T>G	IL17F	Single nucleotide variant (3 prime UTR variant)	Candidiasis, familial, 6 +1 more	GBenign
Select item 357464	NM_052872.4(IL17F):c.*136A>G	IL17F	Single nucleotide variant (3 prime UTR variant)	Candidiasis, familial, 6	GBenign
Select item 357465	NM_052872.4(IL17F):c.*123C>T	IL17F	Single nucleotide variant (3 prime UTR variant)	Candidiasis, familial, 6	GBenign
Select item 357466	NM_052872.4(IL17F):c.482A>G (p.His161Arg)	IL17F (H161R)	Single nucleotide variant (missense variant)	Candidiasis, familial, 6 +1 more	GBenign
Select item 357467	NM_052872.4(IL17F):c.469C>T (p.Pro157Ser)	IL17F (P157S)	Single nucleotide variant (missense variant)	Candidiasis, familial, 6 +1 more	GUncertain significance
Select item 357468	NM_052872.4(IL17F):c.463G>A (p.Val155Ile)	IL17F (V155I)	Single nucleotide variant (missense variant)	Candidiasis, familial, 6 +2 more	GBenign
Select item 910270	NM_052872.4(IL17F):c.456C>T (p.Cys152=)	IL17F	Single nucleotide variant (synonymous variant)	Candidiasis, familial, 6	GConflicting classifications of pathogenicity
Select item 911489	NM_052872.4(IL17F):c.427T>C (p.Leu143=)	IL17F	Single nucleotide variant (synonymous variant)	Candidiasis, familial, 6	GConflicting classifications of pathogenicity
Select item 357469	NM_052872.4(IL17F):c.377A>G (p.Glu126Gly)	IL17F (E126G)	Single nucleotide variant (missense variant)	not provided +2 more	GBenign
Select item 357470	NM_052872.4(IL17F):c.318C>T (p.Gly106=)	IL17F	Single nucleotide variant (synonymous variant)	Candidiasis, familial, 6	GBenign
Select item 911490	NM_052872.4(IL17F):c.254+10A>G	IL17F	Single nucleotide variant (intron variant)	Candidiasis, familial, 6	GUncertain significance
Select item 911491	NM_052872.4(IL17F):c.254+1G>A	IL17F	Single nucleotide variant (splice donor variant)	Candidiasis, familial, 6	GConflicting classifications of pathogenicity
Select item 225391	NM_052872.4(IL17F):c.254+1G>T	IL17F	Single nucleotide variant (splice donor variant)	Candidiasis, familial, 6	GConflicting classifications of pathogenicity
Select item 357471	NM_052872.4(IL17F):c.243C>G (p.Pro81=)	IL17F	Single nucleotide variant (synonymous variant)	Candidiasis, familial, 6	GConflicting classifications of pathogenicity
Select item 357472	NM_052872.4(IL17F):c.223G>A (p.Glu75Lys)	IL17F (E75K)	Single nucleotide variant (missense variant)	Candidiasis, familial, 6	GUncertain significance
Select item 908518	NM_052872.4(IL17F):c.200G>A (p.Arg67His)	IL17F (R67H)	Single nucleotide variant (missense variant)	Candidiasis, familial, 6	GUncertain significance
Select item 357473	NM_052872.4(IL17F):c.-6C>T	IL17F	Single nucleotide variant (5 prime UTR variant)	Candidiasis, familial, 6	GUncertain significance
Select item 357474	NM_052872.4(IL17F):c.-48T>C	IL17F	Single nucleotide variant (5 prime UTR variant)	Candidiasis, familial, 6	GBenign