Related gene-specific medical variations for Gene (Select 55101) - ClinVar - NCBI

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Items: 14

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3272343	NM_018035.3(DMAC2):c.706T>G (p.Trp236Gly)	DMAC2, LOC110121465 (L169R +4 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 3272339	NM_018035.3(DMAC2):c.746G>C (p.Arg249Pro)	DMAC2, LOC110121465 (R255P +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3082998	NM_018035.3(DMAC2):c.763G>A (p.Val255Ile)	DMAC2, LOC110121465 (V234I +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GLikely benign
Select item 3082996	NM_018035.3(DMAC2):c.746G>A (p.Arg249Gln)	DMAC2, LOC110121465 (R249Q +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GLikely benign
Select item 3082995	NM_018035.3(DMAC2):c.719T>C (p.Leu240Pro)	DMAC2, LOC110121465 (L246P +3 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 3082994	NM_018035.3(DMAC2):c.709G>A (p.Ala237Thr)	DMAC2, LOC110121465 (G170D +4 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 3082993	NM_018035.3(DMAC2):c.692T>C (p.Val231Ala)	DMAC2, LOC110121465 (V204A +3 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 3082992	NM_018035.3(DMAC2):c.687C>T (p.Cys229=)	DMAC2, LOC110121465 (A181V +4 more)	Single nucleotide variant (synonymous variant +4 more)	not specified	GLikely benign
Select item 3082991	NM_018035.3(DMAC2):c.684T>A (p.Asn228Lys)	DMAC2, LOC110121465 (I174N +8 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3082990	NM_018035.3(DMAC2):c.621G>A (p.Ser207=)	DMAC2, LOC110121465 (R159Q +4 more)	Single nucleotide variant (synonymous variant +3 more)	not specified	GLikely benign
Select item 3082989	NM_018035.3(DMAC2):c.601C>T (p.Leu201Phe)	DMAC2, LOC110121465 (L201F +4 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2554116	NM_018035.3(DMAC2):c.615C>T (p.Asp205=)	DMAC2, LOC110121465 (T124I +4 more)	Single nucleotide variant (synonymous variant +3 more)	not specified	GLikely benign
Select item 2465418	NM_018035.3(DMAC2):c.683A>G (p.Asn228Ser)	DMAC2, LOC110121465 (I147V +7 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 684521	NM_018035.3(DMAC2):c.688G>A (p.Glu230Lys)	DMAC2, LOC110121465 (E203K +4 more)	Single nucleotide variant (missense variant +3 more)	not provided	Gnot provided