"Ambry Genetics"[submitter] AND "GRB7"[gene] - ClinVar

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Items: 37

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3282623	NM_005310.5(GRB7):c.-50G>A	GRB7 (G7E)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2256914	NM_005310.5(GRB7):c.-45G>A	GRB7 (G9R)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3102232	NM_005310.5(GRB7):c.-17T>C	GRB7 (L18P)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2232742	NM_005310.5(GRB7):c.2T>G (p.Met1Arg)	GRB7 (M1R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2317707	NM_005310.5(GRB7):c.68C>A (p.Thr23Asn)	GRB7 (T46N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2398437	NM_005310.5(GRB7):c.97A>G (p.Thr33Ala)	GRB7 (T56A +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3282621	NM_005310.5(GRB7):c.164G>A (p.Arg55Gln)	GRB7 (R78Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2257303	NM_005310.5(GRB7):c.269C>T (p.Ala90Val)	GRB7 (A113V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2336068	NM_005310.5(GRB7):c.298C>T (p.Arg100Cys)	GRB7 (R100C +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3102231	NM_005310.5(GRB7):c.299G>A (p.Arg100His)	GRB7 (R100H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2250470	NM_005310.5(GRB7):c.362G>A (p.Gly121Asp)	GRB7 (G121D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2208263	NM_005310.5(GRB7):c.373C>T (p.Arg125Cys)	GRB7 (R125C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2454378	NM_005310.5(GRB7):c.409G>A (p.Ala137Thr)	GRB7 (A137T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2516551	NM_005310.5(GRB7):c.413T>C (p.Leu138Ser)	GRB7 (L138S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102233	NM_005310.5(GRB7):c.517G>T (p.Val173Leu)	GRB7 (V196L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2225952	NM_005310.5(GRB7):c.523G>A (p.Gly175Arg)	GRB7 (G175R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2367141	NM_005310.5(GRB7):c.545G>A (p.Arg182Gln)	GRB7 (R182Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2528103	NM_005310.5(GRB7):c.601G>C (p.Glu201Gln)	GRB7 (E224Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102234	NM_005310.5(GRB7):c.625G>A (p.Asp209Asn)	GRB7 (D209N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2273359	NM_005310.5(GRB7):c.684C>A (p.Ser228Arg)	GRB7 (S228R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 623431	NM_005310.5(GRB7):c.728G>A (p.Arg243Gln)	GRB7 (R243Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2488309	NM_005310.5(GRB7):c.794C>A (p.Thr265Asn)	GRB7 (T265N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2232366	NM_005310.5(GRB7):c.823G>A (p.Val275Met)	GRB7 (V275M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3282618	NM_005310.5(GRB7):c.838G>A (p.Glu280Lys)	GRB7 (E280K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2334294	NM_005310.5(GRB7):c.853G>A (p.Val285Met)	GRB7 (V285M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2212931	NM_005310.5(GRB7):c.976C>T (p.Arg326Cys)	GRB7 (R326C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2291640	NM_005310.5(GRB7):c.1049A>G (p.Gln350Arg)	GRB7 (Q350R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2360230	NM_005310.5(GRB7):c.1073G>C (p.Cys358Ser)	GRB7 (C381S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102230	NM_005310.5(GRB7):c.1082C>T (p.Ser361Phe)	GRB7 (S361F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3282620	NM_005310.5(GRB7):c.1252G>A (p.Gly418Ser)	GRB7 (G441S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2308552	NM_005310.5(GRB7):c.1303C>T (p.Arg435Cys)	GRB7 (R458C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2320942	NM_005310.5(GRB7):c.1385G>A (p.Arg462Gln)	GRB7 (G433R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2267190	NM_005310.5(GRB7):c.1429G>A (p.Val477Met)	GRB7 (V500M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3282622	NM_005310.5(GRB7):c.1525G>A (p.Val509Met)	GRB7 (V509M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2272101	NM_005310.5(GRB7):c.1559C>T (p.Pro520Leu)	GRB7 (P543L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2367635	NM_005310.5(GRB7):c.1583C>T (p.Thr528Met)	GRB7 (T528M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2394704	NM_005310.5(GRB7):c.1586G>A (p.Arg529Gln)	GRB7 (R552Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 37