Related gene-specific medical variations for Gene (Select 645355) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2681612	NM_001395400.1(TMEM200C):c.441G>A (p.Thr147=)	MIR3976HG, TMEM200C	Single nucleotide variant (synonymous variant)	EBV-positive nodal T- and NK-cell lymphoma	GLikely benign
Select item 2648539	NM_001395400.1(TMEM200C):c.435C>T (p.Ser145=)	MIR3976HG, TMEM200C	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2648538	NM_001395400.1(TMEM200C):c.676_690del (p.Ala226_Ala230del)	MIR3976HG, TMEM200C	Deletion (inframe_deletion)	not provided	GLikely benign
Select item 2648537	NM_001395400.1(TMEM200C):c.963C>G (p.Ala321=)	MIR3976HG, TMEM200C	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2648536	NM_001395400.1(TMEM200C):c.1198A>C (p.Ser400Arg)	MIR3976HG, TMEM200C (S400R)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2648535	NM_001395400.1(TMEM200C):c.1199G>T (p.Ser400Ile)	MIR3976HG, TMEM200C (S400I)	Single nucleotide variant (missense variant)	not provided	GLikely benign

ClinVar