Related gene-specific medical variations for Gene (Select 120114) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2689051	NM_001367949.2(FAT3):c.5038G>A (p.Val1680Ile)	FAT3 (V1680I)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1809462	GRCh37/hg19 11q14.3(chr11:92272650-92435173)x1	FAT3	Copy number loss	not provided	GUncertain significance
Select item 1527867	NM_001367949.2(FAT3):c.1091T>C (p.Ile364Thr)	FAT3 (I364T)	Single nucleotide variant (missense variant)	Global developmental delay	GUncertain significance
Select item 980965	GRCh37/hg19 11q14.3(chr11:92015938-92476178)x1	FAT3	Copy number loss	not provided	GLikely benign
Select item 980964	GRCh37/hg19 11q14.3(chr11:91553293-92582340)x3	FAT3	Copy number gain	not provided	GLikely benign
Select item 687778	GRCh37/hg19 11q14.3(chr11:92158870-92601166)x1	FAT3	Copy number loss	not provided	GUncertain significance

ClinVar