"Genome-Nilou Lab"[submitter] AND "CUX1"[gene] - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1255424	NM_181552.4(CUX1):c.190-29T>C	CUX1	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 1255425	NM_181552.4(CUX1):c.269-38T>G	CUX1, LOC126860126	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 1255426	NM_181552.4(CUX1):c.269-34C>A	CUX1, LOC126860126	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 1255427	NM_181552.4(CUX1):c.607+6A>G	CUX1	Single nucleotide variant (intron variant)	Global developmental delay with or without impaired intellectual development +1 more	GBenign
Select item 1255428	NM_181552.4(CUX1):c.674+11C>T	CUX1	Single nucleotide variant (intron variant)	Global developmental delay with or without impaired intellectual development +1 more	GBenign
Select item 1255429	NM_181552.4(CUX1):c.674+31G>A	CUX1	Single nucleotide variant (intron variant)	Global developmental delay with or without impaired intellectual development +1 more	GBenign
Select item 1255430	NM_181552.4(CUX1):c.1104G>A (p.Pro368=)	CUX1	Single nucleotide variant (synonymous variant)	Global developmental delay with or without impaired intellectual development +1 more	GBenign
Select item 1255431	NM_181552.4(CUX1):c.2274A>G (p.Pro758=)	CUX1	Single nucleotide variant (synonymous variant +1 more)	Global developmental delay with or without impaired intellectual development +1 more	GBenign
Select item 1255432	NM_001913.5(CUX1):c.1390G>A (p.Ala464Thr)	CUX1 (A418T +4 more)	Single nucleotide variant (missense variant)	Global developmental delay with or without impaired intellectual development +1 more	GBenign
Select item 1255433	NM_001913.5(CUX1):c.1681-12dup	CUX1	Duplication (intron variant)	Global developmental delay with or without impaired intellectual development	GBenign