"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "NCOR1"[ - ClinVar

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Items: 22

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 735033	NM_006311.4(NCOR1):c.7104G>A (p.Gly2368=)	NCOR1, TTC19	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 726341	NM_006311.4(NCOR1):c.7074A>G (p.Ser2358=)	TTC19, NCOR1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 722211	NM_006311.4(NCOR1):c.6870G>A (p.Met2290Ile)	NCOR1, TTC19 (M2290I +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 771023	NM_006311.4(NCOR1):c.6544G>A (p.Ala2182Thr)	NCOR1 (A2079T +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 722887	NM_006311.4(NCOR1):c.6468G>A (p.Pro2156=)	NCOR1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 784667	NM_006311.4(NCOR1):c.6396G>A (p.Arg2132=)	NCOR1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 710458	NM_006311.4(NCOR1):c.6165C>A (p.Ile2055=)	NCOR1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 712852	NM_006311.4(NCOR1):c.5970G>A (p.Gln1990=)	NCOR1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 723724	NM_006311.4(NCOR1):c.5208C>T (p.Leu1736=)	NCOR1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 793499	NM_006311.4(NCOR1):c.5157G>A (p.Glu1719=)	NCOR1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 777134	NM_006311.4(NCOR1):c.4863A>G (p.Gln1621=)	NCOR1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 747294	NM_006311.4(NCOR1):c.4329C>T (p.Thr1443=)	NCOR1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 777715	NM_006311.4(NCOR1):c.4218A>C (p.Leu1406Phe)	NCOR1 (L1406F +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 768834	NM_006311.4(NCOR1):c.4044G>A (p.Gly1348=)	NCOR1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 716462	NM_006311.4(NCOR1):c.3249G>A (p.Val1083=)	NCOR1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 777135	NM_006311.4(NCOR1):c.2745C>T (p.Leu915=)	NCOR1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 710459	NM_006311.4(NCOR1):c.2513G>C (p.Gly838Ala)	NCOR1 (G838A +2 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 755294	NM_006311.4(NCOR1):c.2055+8T>G	NCOR1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 789340	NM_006311.4(NCOR1):c.1352+8A>G	NCOR1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 735742	NM_006311.4(NCOR1):c.393C>T (p.His131=)	NCOR1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 712853	NM_006311.4(NCOR1):c.96C>T (p.Thr32=)	NCOR1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1484361	NC_000017.10:g.(?_15903163)_(16229212_?)dup	NCOR1, PIGL +1 more	Duplication	not provided	GUncertain significance

ClinVar

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Items: 22