"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "LOC1234 - ClinVar

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Search results

Items: 55

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2203614	NM_001204375.2(NPR3):c.8C>G (p.Ser3Cys)	LOC123493284, NPR3 (S3C)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1630131	NM_001204375.2(NPR3):c.30C>G (p.Ser10=)	LOC123493284, NPR3	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1553626	NM_001204375.2(NPR3):c.30C>T (p.Ser10=)	LOC123493284, NPR3	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1555828	NM_001204375.2(NPR3):c.33G>A (p.Pro11=)	LOC123493284, NPR3	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1949004	NM_001204375.2(NPR3):c.51G>C (p.Trp17Cys)	LOC123493284, NPR3 (W17C)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1617642	NM_001204375.2(NPR3):c.54G>T (p.Ala18=)	LOC123493284, NPR3	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1444599	NM_001204375.2(NPR3):c.57G>C (p.Leu19Phe)	LOC123493284, NPR3 (L19F)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1969249	NM_001204375.2(NPR3):c.63C>G (p.Ala21=)	LOC123493284, NPR3	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3010541	NM_001204375.2(NPR3):c.72C>A (p.Thr24=)	LOC123493284, NPR3	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2955357	NM_001204375.2(NPR3):c.72C>T (p.Thr24=)	LOC123493284, NPR3	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1983907	NM_001204375.2(NPR3):c.86_106del (p.Val29_Gly35del)	LOC123493284, NPR3	Deletion (inframe_deletion +1 more)	not provided	GUncertain significance
Select item 2190864	NM_001204375.2(NPR3):c.90CGG[5] (p.Gly35_Ala36insGly)	LOC123493284, NPR3	Microsatellite (inframe_insertion +1 more)	not provided	GUncertain significance
Select item 1934722	NM_001204375.2(NPR3):c.91G>A (p.Gly31Ser)	LOC123493284, NPR3 (G31S)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1939401	NM_001204375.2(NPR3):c.101G>A (p.Gly34Asp)	LOC123493284, NPR3 (G34D)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1406496	NM_001204375.2(NPR3):c.108G>A (p.Ala36=)	LOC123493284, NPR3	Single nucleotide variant (synonymous variant +1 more)	not provided	GUncertain significance
Select item 1926696	NM_001204375.2(NPR3):c.126C>G (p.Arg42=)	LOC123493284, NPR3	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2012858	NM_001204375.2(NPR3):c.146C>G (p.Pro49Arg)	LOC123493284, NPR3 (P49R)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1369908	NM_001204375.2(NPR3):c.160G>C (p.Glu54Gln)	LOC123493284, NPR3 (E54Q)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1416531	NM_001204375.2(NPR3):c.183G>C (p.Gln61His)	LOC123493284, NPR3 (Q61H)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2840062	NM_001204375.2(NPR3):c.196T>C (p.Leu66=)	LOC123493284, NPR3	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1435491	NM_001204375.2(NPR3):c.218G>A (p.Arg73Gln)	LOC123493284, NPR3 (R73Q)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1233804	NM_001204375.2(NPR3):c.237T>C (p.Ala79=)	LOC123493284, NPR3	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 2034760	NM_001204375.2(NPR3):c.267G>C (p.Gly89=)	LOC123493284, NPR3	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2080201	NM_001204375.2(NPR3):c.272G>C (p.Arg91Pro)	LOC123493284, NPR3 (R91P)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2073147	NM_001204375.2(NPR3):c.272G>T (p.Arg91Leu)	LOC123493284, NPR3 (R91L)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +1 more	GUncertain significance
Select item 1444170	NM_001204375.2(NPR3):c.274C>T (p.Leu92Phe)	LOC123493284, NPR3 (L92F)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2804428	NM_001204375.2(NPR3):c.285G>A (p.Pro95=)	LOC123493284, NPR3	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1376431	NM_001204375.2(NPR3):c.292C>G (p.Arg98Gly)	LOC123493284, NPR3 (R98G)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1653973	NM_001204375.2(NPR3):c.309C>T (p.Tyr103=)	NPR3, LOC123493284	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1657382	NM_001204375.2(NPR3):c.330C>T (p.Asn110=)	LOC123493284, NPR3	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2015311	NM_001204375.2(NPR3):c.342_347del (p.Phe114_Ser115del)	LOC123493284, NPR3	Deletion (inframe_deletion +1 more)	not provided	GUncertain significance
Select item 2032448	NM_001204375.2(NPR3):c.366G>A (p.Ala122=)	NPR3, LOC123493284	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2031145	NM_001204375.2(NPR3):c.387C>T (p.Asp129=)	LOC123493284, NPR3	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1581695	NM_001204375.2(NPR3):c.417A>G (p.Ala139=)	LOC123493284, NPR3	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2900510	NM_001204375.2(NPR3):c.447C>T (p.His149=)	LOC123493284, NPR3	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2784030	NM_001204375.2(NPR3):c.468G>A (p.Ser156=)	LOC123493284, NPR3	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1602691	NM_001204375.2(NPR3):c.516G>T (p.Ser172=)	LOC123493284, NPR3	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1923835	NM_001204375.2(NPR3):c.533C>A (p.Ala178Glu)	LOC123493284, NPR3 (A178E)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1483584	NM_001204375.2(NPR3):c.550A>T (p.Met184Leu)	LOC123493284, NPR3 (M184L)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1385919	NM_001204375.2(NPR3):c.583C>T (p.His195Tyr)	LOC123493284, NPR3 (H195Y)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2906051	NM_001204375.2(NPR3):c.603A>G (p.Ala201=)	LOC123493284, NPR3	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1583943	NM_001204375.2(NPR3):c.657G>A (p.Gly219=)	LOC123493284, NPR3	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1387753	NM_001204375.2(NPR3):c.683G>A (p.Gly228Asp)	LOC123493284, NPR3 (G228D)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 1376340	NM_001204375.2(NPR3):c.688C>T (p.His230Tyr)	LOC123493284, NPR3 (H230Y)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 1440863	NM_001204375.2(NPR3):c.692C>A (p.Thr231Lys)	LOC123493284, NPR3 (T231K)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2179123	NM_001204375.2(NPR3):c.693G>A (p.Thr231=)	LOC123493284, NPR3	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1496287	NM_001204375.2(NPR3):c.712G>C (p.Glu238Gln)	LOC123493284, NPR3 (E238Q)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1461007	NM_001204375.2(NPR3):c.760A>G (p.Ser254Gly)	LOC123493284, NPR3 (S254G)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1519290	NM_001204375.2(NPR3):c.763G>C (p.Glu255Gln)	LOC123493284, NPR3 (E255Q)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 1571423	NM_001204375.2(NPR3):c.765G>A (p.Glu255=)	LOC123493284, NPR3	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2714176	NM_001204375.2(NPR3):c.769+8G>C	LOC123493284, NPR3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1937092	NM_001204375.2(NPR3):c.769+17CCCGGGC[3]	LOC123493284, NPR3	Microsatellite (intron variant)	not provided	GLikely benign
Select item 1938366	NM_001204375.2(NPR3):c.769+17C>A	LOC123493284, NPR3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1926849	NM_001204375.2(NPR3):c.769+18C>G	NPR3, LOC123493284	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2972763	NM_001204375.2(NPR3):c.769+20G>C	LOC123493284, NPR3	Single nucleotide variant (intron variant)	not provided	GLikely benign

ClinVar

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Items: 55