"Ambry Genetics"[submitter] AND "LOC126805632"[gene] - ClinVar - NCBI

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Items: 8

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3191922	NM_003443.3(ZBTB17):c.2254G>A (p.Asp752Asn)	LOC126805632, ZBTB17 (D676N +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2482584	NM_003443.3(ZBTB17):c.2222C>T (p.Ala741Val)	LOC126805632, ZBTB17 (A678V +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3191921	NM_003443.3(ZBTB17):c.2210G>A (p.Arg737Gln)	LOC126805632, ZBTB17 (R655Q +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2249984	NM_003443.3(ZBTB17):c.2135A>G (p.Asn712Ser)	LOC126805632, ZBTB17 (N630S +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3191920	NM_003443.3(ZBTB17):c.2083C>G (p.Leu695Val)	LOC126805632, ZBTB17 (L695V +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2356825	NM_003443.3(ZBTB17):c.2030A>G (p.Gln677Arg)	LOC126805632, ZBTB17 (Q601R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2281480	NM_003443.3(ZBTB17):c.1872C>A (p.Asn624Lys)	LOC126805632, ZBTB17 (N542K +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2508090	NM_003443.3(ZBTB17):c.1702G>A (p.Val568Ile)	LOC126805632, ZBTB17 (V486I +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance