"Ambry Genetics"[submitter] AND "LOC126805641"[gene] - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3330719	NM_020765.3(UBR4):c.10434A>C (p.Lys3478Asn)	LOC126805641, UBR4 (K3478N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2564912	NM_020765.3(UBR4):c.10387C>T (p.Arg3463Cys)	LOC126805641, UBR4 (R3463C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2347963	NM_020765.3(UBR4):c.10348C>G (p.Leu3450Val)	LOC126805641, UBR4 (L3450V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185800	NM_020765.3(UBR4):c.10282G>A (p.Ala3428Thr)	LOC126805641, UBR4 (A3428T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185799	NM_020765.3(UBR4):c.10274G>A (p.Arg3425His)	LOC126805641, UBR4 (R3425H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2555413	NM_020765.3(UBR4):c.10238G>A (p.Arg3413His)	LOC126805641, UBR4 (R3413H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2551589	NM_020765.3(UBR4):c.10218A>C (p.Glu3406Asp)	LOC126805641, UBR4 (E3406D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2268462	NM_020765.3(UBR4):c.10205T>C (p.Phe3402Ser)	LOC126805641, UBR4 (F3402S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2536605	NM_020765.3(UBR4):c.10180G>A (p.Ala3394Thr)	LOC126805641, UBR4 (A3394T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185798	NM_020765.3(UBR4):c.10157G>A (p.Ser3386Asn)	LOC126805641, UBR4 (S3386N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance