Related gene-specific medical variations for Gene (Select 96764) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3455978	NM_024831.8(TGS1):c.15G>C (p.Lys5Asn)	LOC130000400, TGS1 (K5N)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3455972	NM_024831.8(TGS1):c.40C>T (p.Leu14Phe)	LOC130000400, TGS1 (L14F)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3455970	NM_024831.8(TGS1):c.65G>T (p.Cys22Phe)	LOC130000400, TGS1 (C22F)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3455964	NM_024831.8(TGS1):c.59A>C (p.Glu20Ala)	LOC130000400, TGS1 (E20A)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3176809	NM_024831.8(TGS1):c.55C>G (p.Arg19Gly)	LOC130000400, TGS1 (R19G)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2522312	NM_024831.8(TGS1):c.31G>C (p.Glu11Gln)	LOC130000400, TGS1 (E11Q)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2393935	NM_024831.8(TGS1):c.59A>T (p.Glu20Val)	LOC130000400, TGS1 (E20V)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance

ClinVar