ID4[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 13

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2373383	NM_001546.4(ID4):c.55G>A (p.Gly19Ser)	ID4 (G19S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3108004	NM_001546.4(ID4):c.71C>T (p.Ala24Val)	ID4 (A24V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2483198	NM_001546.4(ID4):c.100A>T (p.Ser34Cys)	ID4 (S34C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3107998	NM_001546.4(ID4):c.104T>G (p.Leu35Arg)	ID4 (L35R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2341137	NM_001546.4(ID4):c.124G>A (p.Ala42Thr)	ID4 (A42T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2569060	NM_001546.4(ID4):c.134C>T (p.Ala45Val)	ID4 (A45V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3107999	NM_001546.4(ID4):c.145C>T (p.Arg49Cys)	ID4 (R49C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3108000	NM_001546.4(ID4):c.260A>C (p.Lys87Thr)	ID4 (K87T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3108001	NM_001546.4(ID4):c.352C>G (p.Pro118Ala)	ID4 (P118A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3108002	NM_001546.4(ID4):c.365C>G (p.Ala122Gly)	ID4 (A122G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3108003	NM_001546.4(ID4):c.389C>T (p.Thr130Ile)	ID4 (T130I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2244020	NM_001546.4(ID4):c.437A>C (p.Asp146Ala)	ID4 (D146A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 394079	GRCh37/hg19 6p22.3(chr6:19687791-19839727)x3	ID4	Copy number gain	See cases	GBenign