"GeneDx"[submitter] AND "FAT3"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 58918	GRCh38/hg38 11q14.1-22.3(chr11:78232836-106779420)x1	LINC02553, LINC02700 +528 more	Copy number loss	See cases	GPathogenic
Select item 58919	GRCh38/hg38 11q14.1-22.2(chr11:85242847-102920097)x1	LOC101929174, LOC102723838 +378 more	Copy number loss	See cases	GPathogenic
Select item 1268011	NM_001367949.2(FAT3):c.2899C>T (p.Leu967=)	FAT3	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 145253	GRCh38/hg38 11q14.3(chr11:92560681-92664445)x1	FAT3, LOC126861292	Copy number loss	See cases	GBenign
Select item 1246514	NM_001367949.2(FAT3):c.5177A>G (p.Gln1726Arg)	FAT3 (Q1726R)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 1334324	NM_001367949.2(FAT3):c.6498T>C (p.Pro2166=)	FAT3	Single nucleotide variant (synonymous variant)	not provided	GBenign

ClinVar