"Ambry Genetics"[submitter] AND "LOC126806059"[gene] - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2233314	NM_015014.4(RBM34):c.364A>G (p.Arg122Gly)	LOC126806059, RBM34 (R122G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2616499	NM_015014.4(RBM34):c.326A>G (p.Lys109Arg)	LOC126806059, RBM34 (K109R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2329033	NM_015014.4(RBM34):c.286A>G (p.Arg96Gly)	LOC126806059, RBM34 (R96G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2563756	NM_015014.4(RBM34):c.281T>C (p.Ile94Thr)	LOC126806059, RBM34 (I94T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3152338	NM_015014.4(RBM34):c.250C>T (p.Arg84Trp)	LOC126806059, RBM34 (R84W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2456009	NM_015014.4(RBM34):c.232A>G (p.Thr78Ala)	LOC126806059, RBM34 (T78A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2215499	NM_015014.4(RBM34):c.198G>C (p.Gln66His)	LOC126806059, RBM34 (Q66H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2587971	NM_015014.4(RBM34):c.44T>C (p.Val15Ala)	LOC126806059, RBM34 (V15A)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2365107	NM_015014.4(RBM34):c.36G>T (p.Lys12Asn)	LOC126806059, RBM34 (K12N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2622070	NM_015014.4(RBM34):c.9G>T (p.Leu3Phe)	LOC126806059, RBM34 (L3F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance