"Fulgent Genetics, Fulgent Genetics"[submitter] AND "DLC1"[gene] - ClinVar - NCBI

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1328014	NM_182643.3(DLC1):c.3856-6G>A	LOC126860305, DLC1	Single nucleotide variant (intron variant)	not provided +1 more	GBenign/Likely benign
Select item 737441	NM_182643.3(DLC1):c.3609C>A (p.Thr1203=)	DLC1	Single nucleotide variant (synonymous variant)	Colorectal cancer +1 more	GLikely benign
Select item 736557	NM_182643.3(DLC1):c.3327+8C>T	DLC1	Single nucleotide variant (intron variant)	Colorectal cancer +1 more	GLikely benign
Select item 430439	NM_182643.3(DLC1):c.2753G>C (p.Arg918Pro)	DLC1 (R918P +3 more)	Single nucleotide variant (missense variant)	Colorectal cancer +1 more	GUncertain significance
Select item 1596118	NM_182643.3(DLC1):c.2265G>C (p.Thr755=)	DLC1	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 781117	NM_182643.3(DLC1):c.2199C>T (p.Ser733=)	DLC1	Single nucleotide variant (synonymous variant)	Colorectal cancer +1 more	GBenign
Select item 729939	NM_182643.3(DLC1):c.2147T>C (p.Ile716Thr)	DLC1 (I313T +3 more)	Single nucleotide variant (missense variant)	Colorectal cancer +1 more	GLikely benign
Select item 1511026	NM_182643.3(DLC1):c.1700C>T (p.Pro567Leu)	DLC1 (P164L +3 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 789014	NM_182643.3(DLC1):c.1530G>A (p.Ala510=)	DLC1	Single nucleotide variant (5 prime UTR variant +1 more)	Colorectal cancer +1 more	GBenign
Select item 740487	NM_182643.3(DLC1):c.1348+9A>C	DLC1 (T453P)	Single nucleotide variant (missense variant +1 more)	Colorectal cancer +1 more	GLikely benign
Select item 432679	NM_182643.3(DLC1):c.857A>G (p.Asn286Ser)	DLC1 (N286S)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 1640474	NM_182643.3(DLC1):c.167A>G (p.Glu56Gly)	DLC1 (E56G)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GLikely benign