Related gene-specific medical variations for Gene (Select 10475) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3328723	NM_006355.5(TRIM38):c.600G>T (p.Arg200Ser)	LOC126859624, TRIM38 (R200S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3182422	NM_006355.5(TRIM38):c.592C>A (p.Leu198Ile)	LOC126859624, TRIM38 (L198I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2596798	NM_006355.5(TRIM38):c.672T>A (p.Asn224Lys)	LOC126859624, TRIM38 (N224K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2494689	NM_006355.5(TRIM38):c.602T>C (p.Leu201Pro)	LOC126859624, TRIM38 (L201P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2321960	NM_006355.5(TRIM38):c.538C>T (p.Arg180Trp)	LOC126859624, TRIM38 (R180W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2293622	NM_006355.5(TRIM38):c.707A>G (p.Lys236Arg)	LOC126859624, TRIM38 (K236R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar