Related gene-specific medical variations for Gene (Select 3574) - ClinVar - NCBI

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Items: 18

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3334006	NM_016010.3(ZC2HC1A):c.517G>T (p.Ala173Ser)	IL7, ZC2HC1A (A173S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3192227	NM_016010.3(ZC2HC1A):c.446G>C (p.Ser149Thr)	IL7, ZC2HC1A (S149T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2672195	NM_016010.3(ZC2HC1A):c.382A>T (p.Arg128Ter)	IL7, ZC2HC1A (R128*)	Single nucleotide variant (nonsense +1 more)	not provided	GUncertain significance
Select item 2658671	NM_016010.3(ZC2HC1A):c.605-5A>G	IL7, ZC2HC1A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2612204	NM_016010.3(ZC2HC1A):c.587C>A (p.Ala196Asp)	IL7, ZC2HC1A (A196D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2605509	NM_016010.3(ZC2HC1A):c.502G>C (p.Val168Leu)	IL7, ZC2HC1A (V168L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2592974	NM_016010.3(ZC2HC1A):c.581G>A (p.Ser194Asn)	IL7, ZC2HC1A (S194N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2589650	NM_016010.3(ZC2HC1A):c.244A>G (p.Arg82Gly)	IL7, ZC2HC1A (R82G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2509875	NM_016010.3(ZC2HC1A):c.263T>C (p.Ile88Thr)	IL7, ZC2HC1A (I88T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2509286	NM_016010.3(ZC2HC1A):c.517G>A (p.Ala173Thr)	IL7, ZC2HC1A (A173T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2464974	NM_016010.3(ZC2HC1A):c.328C>T (p.Pro110Ser)	IL7, ZC2HC1A (P110S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2463392	NM_016010.3(ZC2HC1A):c.586G>A (p.Ala196Thr)	IL7, ZC2HC1A (A196T)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2372000	NM_016010.3(ZC2HC1A):c.494G>A (p.Arg165Gln)	IL7, ZC2HC1A (R165Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2364394	NM_016010.3(ZC2HC1A):c.566G>A (p.Arg189Gln)	IL7, ZC2HC1A (R189Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2341799	NM_016010.3(ZC2HC1A):c.440G>A (p.Arg147His)	IL7, ZC2HC1A (R147H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2221285	NM_016010.3(ZC2HC1A):c.206C>T (p.Pro69Leu)	IL7, ZC2HC1A (P69L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2215861	NM_016010.3(ZC2HC1A):c.473C>T (p.Thr158Ile)	IL7, ZC2HC1A (T158I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2206500	NM_016010.3(ZC2HC1A):c.136C>T (p.Arg46Trp)	IL7, ZC2HC1A (R46W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance