Related gene-specific medical variations for Gene (Select 23705) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2642393	NM_001301043.2(CADM1):c.1023AAC[1] (p.Thr353del)	CADM1, LOC126861346 (T353del)	Microsatellite (inframe_deletion +1 more)	not provided	GLikely benign
Select item 1809228	GRCh37/hg19 11q23.3(chr11:115016471-115222588)x3	CADM1	Copy number gain	not provided	GUncertain significance
Select item 782217	NM_001301043.2(CADM1):c.1007C>T (p.Thr336Ile)	CADM1, LOC126861346 (T336I)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 776659	NM_001301043.2(CADM1):c.1028CCA[12] (p.Thr353dup)	CADM1, LOC126861346	Microsatellite (inframe_insertion +1 more)	not provided	GLikely benign
Select item 761544	NM_001301043.2(CADM1):c.995-5T>C	CADM1, LOC126861346	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 733505	NM_001301043.2(CADM1):c.1028CCA[8] (p.Thr351_Thr353del)	CADM1, LOC126861346	Microsatellite (inframe_deletion +1 more)	not provided	GBenign
Select item 563804	GRCh37/hg19 11q23.3(chr11:115187860-115238060)x1	CADM1	Copy number loss	not provided	GUncertain significance
Select item 441958	GRCh37/hg19 11q23.3(chr11:115101293-115320089)x1	CADM1	Copy number loss	See cases	GUncertain significance

ClinVar