Related gene-specific medical variations for Gene (Select 55281) - ClinVar - NCBI

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Items: 14

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3326794	NM_018295.5(TMEM140):c.544C>A (p.Leu182Ile)	CYREN, TMEM140 (L182I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3326793	NM_018295.5(TMEM140):c.61G>C (p.Val21Leu)	CYREN, TMEM140 (V21L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3178806	NM_018295.5(TMEM140):c.7G>A (p.Gly3Ser)	CYREN, TMEM140 (G3S)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3178805	NM_018295.5(TMEM140):c.521G>A (p.Arg174Lys)	CYREN, TMEM140 (R174K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3178803	NM_018295.5(TMEM140):c.289G>T (p.Ala97Ser)	CYREN, TMEM140 (A97S)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3178802	NM_018295.5(TMEM140):c.142G>A (p.Gly48Ser)	CYREN, TMEM140 (G48S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3178801	NM_018295.5(TMEM140):c.123C>A (p.Asp41Glu)	CYREN, TMEM140 (D41E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2488078	NM_018295.5(TMEM140):c.268T>C (p.Ser90Pro)	CYREN, TMEM140 (S90P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2482685	NM_018295.5(TMEM140):c.313C>G (p.Gln105Glu)	CYREN, TMEM140 (Q105E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2406402	NM_018295.5(TMEM140):c.388G>A (p.Gly130Ser)	CYREN, TMEM140 (G130S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2390552	NM_018295.5(TMEM140):c.265G>A (p.Gly89Arg)	CYREN, TMEM140 (G89R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2383473	NM_018295.5(TMEM140):c.170A>G (p.Glu57Gly)	CYREN, TMEM140 (E57G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2364880	NM_018295.5(TMEM140):c.295C>A (p.Gln99Lys)	CYREN, TMEM140 (Q99K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2294213	NM_018295.5(TMEM140):c.479T>C (p.Leu160Ser)	CYREN, TMEM140 (L160S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance