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

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Items: 45

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 733657	NM_007124.3(UTRN):c.687T>C (p.Asp229=)	UTRN	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 791267	NM_007124.3(UTRN):c.964C>T (p.Leu322=)	UTRN	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 733691	NM_007124.3(UTRN):c.2197-4G>T	UTRN	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 780649	NM_007124.3(UTRN):c.2337A>G (p.Glu779=)	UTRN	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 710329	NM_007124.3(UTRN):c.2539A>C (p.Asn847His)	UTRN (N847H)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 771867	NM_007124.3(UTRN):c.2654G>A (p.Arg885His)	UTRN (R885H)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 778924	NM_007124.3(UTRN):c.2746T>C (p.Leu916=)	UTRN	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 724092	NM_007124.3(UTRN):c.2837C>T (p.Ala946Val)	UTRN (A946V)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 723484	NM_007124.3(UTRN):c.3139G>A (p.Gly1047Arg)	LOC126859819, UTRN (G1047R)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 764083	NM_007124.3(UTRN):c.3180+9T>G	LOC126859819, UTRN	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 780664	NM_007124.3(UTRN):c.3399C>T (p.Asp1133=)	UTRN	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 782842	NM_007124.3(UTRN):c.3771G>A (p.Lys1257=)	UTRN	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 773202	NM_007124.3(UTRN):c.4247A>G (p.Gln1416Arg)	UTRN (Q1416R)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 718534	NM_007124.3(UTRN):c.4437+9T>C	UTRN	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 715574	NM_007124.3(UTRN):c.4594-8C>T	UTRN	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 715575	NM_007124.3(UTRN):c.4626A>C (p.Ala1542=)	UTRN	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 715576	NM_007124.3(UTRN):c.4682C>G (p.Ser1561Cys)	UTRN (S1561C)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 715403	NM_007124.3(UTRN):c.4874G>A (p.Arg1625Lys)	UTRN (R1625K)	Single nucleotide variant (missense variant)	not specified +1 more	GLikely benign
Select item 713222	NM_007124.3(UTRN):c.4959G>A (p.Gln1653=)	UTRN	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 784100	NM_007124.3(UTRN):c.5525G>A (p.Arg1842Lys)	UTRN (R1842K)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 717216	NM_007124.3(UTRN):c.5585G>A (p.Gly1862Glu)	UTRN (G1862E)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 758232	NM_007124.3(UTRN):c.5634A>C (p.Lys1878Asn)	UTRN (K1878N)	Single nucleotide variant (missense variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 783476	NM_007124.3(UTRN):c.5689A>C (p.Thr1897Pro)	UTRN (T1897P)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 731378	NM_007124.3(UTRN):c.5734-10A>G	UTRN	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 781758	NM_007124.3(UTRN):c.5745C>T (p.Asp1915=)	UTRN	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 778265	NM_007124.3(UTRN):c.5899C>T (p.Arg1967Trp)	UTRN (R1967W)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 777810	NM_007124.3(UTRN):c.6179G>A (p.Gly2060Asp)	UTRN (G2060D)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 731327	NM_007124.3(UTRN):c.6279A>G (p.Leu2093=)	UTRN	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 773472	NM_007124.3(UTRN):c.6388G>A (p.Glu2130Lys)	UTRN (E2130K)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 778925	NM_007124.3(UTRN):c.6468A>G (p.Glu2156=)	UTRN	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 784101	NM_007124.3(UTRN):c.6664A>G (p.Thr2222Ala)	UTRN (T2222A)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 716638	NM_007124.3(UTRN):c.6679A>G (p.Ile2227Val)	UTRN (I2227V)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 789185	NM_007124.3(UTRN):c.6864A>C (p.Thr2288=)	UTRN	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 713896	NM_007124.3(UTRN):c.7617A>G (p.Arg2539=)	UTRN	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 730771	NM_007124.3(UTRN):c.7926A>G (p.Leu2642=)	UTRN	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 751598	NM_007124.3(UTRN):c.8133G>A (p.Glu2711=)	UTRN	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 712639	NM_007124.3(UTRN):c.8253G>A (p.Thr2751=)	UTRN	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 721076	NM_007124.3(UTRN):c.8451G>A (p.Pro2817=)	UTRN	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 746347	NM_007124.3(UTRN):c.8944C>T (p.Pro2982Ser)	LOC123864093, UTRN (P2982S +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 715252	NM_007124.3(UTRN):c.8960A>T (p.Asp2987Val)	LOC123864093, UTRN (D542V +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 773732	NM_007124.3(UTRN):c.8988T>C (p.His2996=)	LOC123864093, UTRN	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 728617	NM_007124.3(UTRN):c.9342G>A (p.Val3114=)	UTRN	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 725160	NM_007124.3(UTRN):c.9903G>A (p.Ser3301=)	UTRN	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 738473	NM_007124.3(UTRN):c.10179G>A (p.Ala3393=)	UTRN	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 740816	NM_007124.3(UTRN):c.10293+7G>A	UTRN	Single nucleotide variant (intron variant)	not provided	GLikely benign

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Items: 45