"Ambry Genetics"[submitter] AND "LRRTM4"[gene] - ClinVar - NCBI

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Items: 15

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2207859	NM_001134745.3(LRRTM4):c.1727C>T (p.Ala576Val)	LRRTM4 (A577V +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2355751	NM_001134745.3(LRRTM4):c.1663C>G (p.Pro555Ala)	LRRTM4 (P555A +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2538880	NM_001134745.3(LRRTM4):c.1369C>G (p.Leu457Val)	LRRTM4 (L457V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2313397	NM_001134745.3(LRRTM4):c.1334T>C (p.Val445Ala)	LRRTM4 (V446A +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2341013	NM_001134745.3(LRRTM4):c.1331A>G (p.Tyr444Cys)	LRRTM4 (Y444C +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2369622	NM_001134745.3(LRRTM4):c.872A>G (p.Asn291Ser)	LRRTM4 (N291S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2335362	NM_001134745.3(LRRTM4):c.847A>G (p.Asn283Asp)	LRRTM4 (N283D +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2298492	NM_001134745.3(LRRTM4):c.750G>T (p.Trp250Cys)	LRRTM4 (W251C +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2336531	NM_001134745.3(LRRTM4):c.520A>G (p.Ile174Val)	LRRTM4 (I175V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2333449	NM_001134745.3(LRRTM4):c.417C>A (p.Asp139Glu)	LRRTM4 (D140E +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2333448	NM_001134745.3(LRRTM4):c.416A>C (p.Asp139Ala)	LRRTM4 (D140A +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2510865	NM_001134745.3(LRRTM4):c.376A>G (p.Asn126Asp)	LRRTM4 (N126D +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2239461	NM_001134745.3(LRRTM4):c.85G>A (p.Gly29Ser)	LRRTM4 (G29S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2368056	NM_001134745.3(LRRTM4):c.38G>A (p.Ser13Asn)	LRRTM4 (S13N +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2538676	NM_001134745.3(LRRTM4):c.34A>G (p.Met12Val)	LRRTM4 (M12V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance