ClinVar for Gene (Select 55801) - ClinVar

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Links from Gene

Items: 29

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3285848	NM_018402.2(IL26):c.65A>C (p.Lys22Thr)	IL26 (K22T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3109347	NM_018402.2(IL26):c.284G>C (p.Gly95Ala)	IL26 (G95A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3109346	NM_018402.2(IL26):c.172G>A (p.Glu58Lys)	IL26 (E58K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3109344	NM_018402.2(IL26):c.161C>T (p.Ala54Val)	IL26 (A54V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2685437	GRCh37/hg19 12q14.1-15(chr12:61755618-70035424)x1	AVPR1A, C12orf56 +40 more	Copy number loss	not provided	GPathogenic
Select item 2617555	NM_018402.2(IL26):c.383C>G (p.Ala128Gly)	IL26 (A128G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2555445	NM_018402.2(IL26):c.302G>C (p.Gly101Ala)	IL26 (G101A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2526155	NM_018402.2(IL26):c.339C>A (p.Ser113Arg)	IL26 (S113R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2515966	NM_018402.2(IL26):c.245A>G (p.Gln82Arg)	IL26 (Q82R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2465173	NM_018402.2(IL26):c.97T>C (p.Tyr33His)	IL26 (Y33H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2356505	NM_018402.2(IL26):c.404C>A (p.Thr135Asn)	IL26 (T135N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2340987	NM_018402.2(IL26):c.296T>C (p.Leu99Ser)	IL26 (L99S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2293592	NM_018402.2(IL26):c.404C>T (p.Thr135Ile)	IL26 (T135I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2261572	NM_018402.2(IL26):c.197T>C (p.Leu66Ser)	IL26 (L66S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2245726	NM_018402.2(IL26):c.189T>G (p.Asn63Lys)	IL26 (N63K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2236268	NM_018402.2(IL26):c.161C>A (p.Ala54Glu)	IL26 (A54E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1879249	GRCh37/hg19 12q14.2-15(chr12:64609458-70352103)x1	BEST3, C12orf56 +34 more	Copy number loss	not provided	GPathogenic
Select item 1340548	GRCh37/hg19 12q15(chr12:68537457-68698086)x3	IFNG, IL22 +2 more	Copy number gain	not provided	GUncertain significance
Select item 1340105	GRCh37/hg19 12q14.3-15(chr12:66045645-68872343)x1	CAND1, DYRK2 +10 more	Copy number loss	not provided	GPathogenic
Select item 1180525	GRCh37/hg19 12q14.3-21.1(chr12:65251705-75263379)x1	CAND1, RAB3IP +42 more	Copy number loss	not provided	GPathogenic
Select item 980441	GRCh37/hg19 12q15(chr12:68572386-70833868)x1	BEST3, CCT2 +17 more	Copy number loss	not provided	GPathogenic
Select item 776730	NM_018402.2(IL26):c.87C>T (p.Thr29=)	IL26	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 563911	GRCh37/hg19 12q15(chr12:68537456-68698086)x3	IFNG, IL22 +2 more	Copy number gain	not provided	GUncertain significance
Select item 441984	GRCh37/hg19 12p13.33-q24.33(chr12:173787-133777902)	SLC15A5, SLC16A7 +1006 more	Copy number gain	See cases	GPathogenic
Select item 441983	GRCh37/hg19 12p13.33-q24.33(chr12:173787-133777902)x3	A2M, A2ML1 +1006 more	Copy number gain	See cases	GPathogenic
Select item 268075	GRCh37/hg19 12p13.33-q24.33(chr12:1-133851895)x3	GALNT8, H2AJ +1007 more	Copy number gain	See cases	GPathogenic
Select item 154378	GRCh38/hg38 12q14.3-15(chr12:65445176-71026337)x1	IL22, BEST3 +163 more	Copy number loss	See cases	GPathogenic
Select item 150740	GRCh38/hg38 12p13.33-q24.33(chr12:121271-133196807)x3	ACAD10, ACADS +4836 more	Copy number gain	See cases	GPathogenic
Select item 146282	GRCh38/hg38 12q15-21.2(chr12:68011417-75383054)x1	ATXN7L3B, BEST3 +141 more	Copy number loss	See cases	GLikely pathogenic

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Links from Gene

Items: 29