Related gene-specific medical variations for Gene (Select 11130) - ClinVar - NCBI

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Links from Gene

Items: 16

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2611563	NM_007057.4(ZWINT):c.268A>G (p.Ile90Val)	LOC126860936, ZWINT (I90V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2602136	NM_007057.4(ZWINT):c.222G>C (p.Lys74Asn)	LOC126860936, ZWINT (K74N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2558250	NM_007057.4(ZWINT):c.257G>A (p.Arg86Gln)	LOC126860936, ZWINT (R86Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2556840	NM_007057.4(ZWINT):c.383G>C (p.Arg128Pro)	LOC126860936, ZWINT (R128P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2528016	NM_007057.4(ZWINT):c.401C>T (p.Ala134Val)	LOC126860936, ZWINT (A134V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2517747	NM_007057.4(ZWINT):c.325G>T (p.Ala109Ser)	LOC126860936, ZWINT (A109S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2515450	NM_007057.4(ZWINT):c.413T>C (p.Leu138Pro)	LOC126860936, ZWINT (L138P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2328177	NM_007057.4(ZWINT):c.92A>G (p.Glu31Gly)	LOC126860936, ZWINT (E31G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2325169	NM_007057.4(ZWINT):c.111G>T (p.Lys37Asn)	LOC126860936, ZWINT (K37N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2270725	NM_007057.4(ZWINT):c.206A>T (p.Gln69Leu)	LOC126860936, ZWINT (Q69L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2204648	NM_007057.4(ZWINT):c.438G>A (p.Met146Ile)	LOC126860936, ZWINT (M146I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1340657	GRCh37/hg19 10q21.1(chr10:57983532-58173033)x1	ZWINT	Copy number loss	not provided	GLikely benign
Select item 980922	GRCh37/hg19 10q21.1(chr10:57590896-58861610)x3	ZWINT	Copy number gain	not provided	GLikely benign
Select item 815350	GRCh37/hg19 10q21.1(chr10:57969989-59123710)x1	ZWINT	Copy number loss	not provided	GUncertain significance
Select item 715021	NM_007057.4(ZWINT):c.423+8C>T	LOC126860936, ZWINT	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 563724	GRCh37/hg19 10q21.1(chr10:58066037-58321888)x1	ZWINT	Copy number loss	not provided	GLikely benign