"Ambry Genetics"[submitter] AND "MORF4L1"[gene] - ClinVar - NCBI

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2545951	NM_006791.4(MORF4L1):c.28A>G (p.Lys10Glu)	MORF4L1 (K10E)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2326139	NM_006791.4(MORF4L1):c.156-1163G>C	MORF4L1 (R56T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3200236	NM_006791.4(MORF4L1):c.156-1155C>T	MORF4L1 (R59C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2546125	NM_006791.4(MORF4L1):c.156-1143T>A	MORF4L1 (S63T)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2341123	NM_006791.4(MORF4L1):c.156-1100C>G	MORF4L1 (P77R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3200244	NM_006791.4(MORF4L1):c.156-1074C>A	MORF4L1 (P86T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3200249	NM_006791.4(MORF4L1):c.197T>C (p.Val66Ala)	MORF4L1 (V66A +1 more)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2378445	NM_006791.4(MORF4L1):c.368G>C (p.Gly123Ala)	MORF4L1 (G123A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2320295	NM_006791.4(MORF4L1):c.379A>G (p.Ser127Gly)	MORF4L1 (S127G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2357338	NM_006791.4(MORF4L1):c.866A>G (p.Asn289Ser)	MORF4L1 (N328S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2607842	NM_006791.4(MORF4L1):c.902A>G (p.Asn301Ser)	MORF4L1 (N301S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance