Related gene-specific medical variations for Gene (Select 11326) - ClinVar - NCBI

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Items: 14

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3344334	NM_007268.3(VSIG4):c.472G>C (p.Gly158Arg)	LOC126863268, VSIG4 (G158R)	Single nucleotide variant (missense variant +1 more)	VSIG4-related disorder	GUncertain significance
Select item 3332354	NM_007268.3(VSIG4):c.343G>A (p.Val115Ile)	LOC126863268, VSIG4 (V115I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3332352	NM_007268.3(VSIG4):c.584C>A (p.Thr195Asn)	LOC126863268, VSIG4 (T195N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3189130	NM_007268.3(VSIG4):c.290C>T (p.Ser97Phe)	LOC126863268, VSIG4 (S97F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3050273	NM_007268.3(VSIG4):c.603G>A (p.Ala201=)	LOC126863268, VSIG4	Single nucleotide variant (synonymous variant +1 more)	VSIG4-related disorder	GLikely benign
Select item 3047863	NM_007268.3(VSIG4):c.590T>A (p.Leu197His)	LOC126863268, VSIG4 (L197H)	Single nucleotide variant (missense variant +1 more)	VSIG4-related disorder	GLikely benign
Select item 3044903	NM_007268.3(VSIG4):c.322C>T (p.Arg108Trp)	LOC126863268, VSIG4 (R108W)	Single nucleotide variant (missense variant)	VSIG4-related disorder	GBenign
Select item 3034962	NM_007268.3(VSIG4):c.408G>A (p.Gln136=)	LOC126863268, VSIG4	Single nucleotide variant (synonymous variant)	VSIG4-related disorder	GLikely benign
Select item 2620621	NM_007268.3(VSIG4):c.302G>A (p.Ser101Asn)	LOC126863268, VSIG4 (S101N)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2390375	NM_007268.3(VSIG4):c.364G>C (p.Gly122Arg)	LOC126863268, VSIG4 (G122R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2375511	NM_007268.3(VSIG4):c.613G>A (p.Asp205Asn)	LOC126863268, VSIG4 (D205N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2356490	NM_007268.3(VSIG4):c.480G>T (p.Arg160Ser)	LOC126863268, VSIG4 (R160S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 779483	NM_007268.3(VSIG4):c.274G>T (p.Val92Phe)	LOC126863268, VSIG4 (V92F)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 722281	NM_007268.3(VSIG4):c.413-10T>G	LOC126863268, VSIG4	Single nucleotide variant (intron variant)	not provided	GBenign