Related gene-specific medical variations for Gene (Select 93109) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3179502	NM_001011655.3(TMEM44):c.82A>C (p.Ile28Leu)	TMEM44, TMEM44-AS2 (I28L)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3179499	NM_001011655.3(TMEM44):c.71A>G (p.His24Arg)	TMEM44, TMEM44-AS2 (H24R)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3179490	NM_001011655.3(TMEM44):c.1264G>A (p.Ala422Thr)	TMEM44, TMEM44-AS1 (A432T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2613026	NM_001011655.3(TMEM44):c.7G>A (p.Glu3Lys)	LOC129938210, TMEM44 +1 more (E3K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2534686	NM_001011655.3(TMEM44):c.37G>A (p.Asp13Asn)	TMEM44, TMEM44-AS2 (D13N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2534685	NM_001011655.3(TMEM44):c.106G>T (p.Ala36Ser)	TMEM44, TMEM44-AS2 (A36S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2216850	NM_001011655.3(TMEM44):c.38A>C (p.Asp13Ala)	TMEM44, TMEM44-AS2 (D13A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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