Related gene-specific medical variations for Gene (Select 9202) - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3334814	NM_005095.3(ZMYM4):c.429T>A (p.Asp143Glu)	ZMYM4, ZMYM4-AS1 (D143E +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3193809	NM_005095.3(ZMYM4):c.812A>G (p.Lys271Arg)	ZMYM4, ZMYM4-AS1 (K271R +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3193808	NM_005095.3(ZMYM4):c.536G>A (p.Arg179His)	ZMYM4, ZMYM4-AS1 (R147H +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3193807	NM_005095.3(ZMYM4):c.454C>T (p.Arg152Trp)	ZMYM4, ZMYM4-AS1 (R120W +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3193800	NM_005095.3(ZMYM4):c.302T>C (p.Leu101Pro)	ZMYM4, ZMYM4-AS1 (L104P +2 more)	Single nucleotide variant (non-coding transcript variant +3 more)	not specified	GUncertain significance
Select item 3193795	NM_005095.3(ZMYM4):c.253G>A (p.Val85Ile)	ZMYM4, ZMYM4-AS1 (V85I +2 more)	Single nucleotide variant (non-coding transcript variant +3 more)	not specified	GUncertain significance
Select item 2588125	NM_005095.3(ZMYM4):c.743G>T (p.Arg248Ile)	ZMYM4, ZMYM4-AS1 (R216I +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2541716	NM_005095.3(ZMYM4):c.459A>T (p.Lys153Asn)	ZMYM4, ZMYM4-AS1 (K153N +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2319963	NM_005095.3(ZMYM4):c.572A>G (p.Asp191Gly)	ZMYM4, ZMYM4-AS1 (D159G +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2286089	NM_005095.3(ZMYM4):c.1799G>A (p.Arg600His)	LOC129388494, ZMYM4 (R603H +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2229832	NM_005095.3(ZMYM4):c.545G>A (p.Arg182Gln)	ZMYM4, ZMYM4-AS1 (R185Q +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance