"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "CLMN"[g - ClinVar - NCBI

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Items: 19

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 786255	NM_024734.4(CLMN):c.2888C>T (p.Pro963Leu)	CLMN (P963L)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 783696	NM_024734.4(CLMN):c.2840+4G>A	CLMN	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 776857	NM_024734.4(CLMN):c.2698A>T (p.Ile900Phe)	CLMN (I900F)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 779738	NM_024734.4(CLMN):c.2511+10C>T	CLMN	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 770999	NM_024734.4(CLMN):c.2352G>A (p.Ser784=)	CLMN	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 717456	NM_024734.4(CLMN):c.2312A>C (p.Glu771Ala)	CLMN (E771A)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 734935	NM_024734.4(CLMN):c.2199G>A (p.Glu733=)	CLMN	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 787953	NM_024734.4(CLMN):c.1776C>T (p.Asp592=)	CLMN	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 786256	NM_024734.4(CLMN):c.1554C>T (p.His518=)	CLMN	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 783697	NM_024734.4(CLMN):c.1465G>T (p.Val489Phe)	CLMN (V489F)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 714521	NM_024734.4(CLMN):c.1069G>A (p.Glu357Lys)	CLMN (E357K)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 788893	NM_024734.4(CLMN):c.886-13_886-12dup	CLMN	Duplication (intron variant)	not provided	GBenign
Select item 785468	NM_024734.4(CLMN):c.886-4G>T	CLMN	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 784612	NM_024734.4(CLMN):c.826G>A (p.Glu276Lys)	CLMN (E276K)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 740265	NM_024734.4(CLMN):c.370C>G (p.Pro124Ala)	CLMN (P124A)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 779739	NM_024734.4(CLMN):c.333G>T (p.Leu111=)	CLMN	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 736198	NM_024734.4(CLMN):c.144+8C>T	CLMN	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2427518	NC_000014.8:g.(?_95080779)_(97347545_?)dup	AK7, ATG2B +17 more	Duplication	not provided	GUncertain significance
Select item 2425566	NC_000014.8:g.(?_90429459)_(97347545_?)dup	SYNE3, TC2N +66 more	Duplication	not provided	GUncertain significance