"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "MUC16"[ - ClinVar

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Items: 60

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 718464	NM_001401501.2(MUC16):c.44076G>A (p.Glu14692=)	MUC16	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign
Select item 777411	NM_001401501.2(MUC16):c.43638T>G (p.Asp14546Glu)	MUC16 (D13704E +3 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 768966	NM_024690.2(MUC16):c.39648T>C (p.Tyr13216=)	MUC16	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 768967	NM_001401501.2(MUC16):c.39833-5A>T	MUC16	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 768968	NM_001401501.2(MUC16):c.38592T>C (p.Gly12864=)	MUC16	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 781384	NM_001401501.2(MUC16):c.35854C>A (p.Pro11952Thr)	MUC16 (P11912T +2 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 760765	NM_001401501.2(MUC16):c.32527A>G (p.Lys10843Glu)	MUC16 (K10803E +2 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 780174	NM_001401501.2(MUC16):c.32429C>T (p.Thr10810Ile)	MUC16 (T10770I +2 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 780523	NM_001401501.2(MUC16):c.30468A>G (p.Leu10156=)	MUC16	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 720412	NM_001401501.2(MUC16):c.28678G>A (p.Ala9560Thr)	MUC16 (A9520T +2 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 780524	NM_001401501.2(MUC16):c.28404A>G (p.Glu9468=)	MUC16	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 780525	NM_001401501.2(MUC16):c.27438C>G (p.Thr9146=)	MUC16	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 779284	NM_001401501.2(MUC16):c.27150C>T (p.Ser9050=)	MUC16	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 775405	NM_001401501.2(MUC16):c.26792T>C (p.Met8931Thr)	MUC16 (M8891T +2 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 780526	NM_001401501.2(MUC16):c.26513C>T (p.Ser8838Leu)	MUC16 (S8798L +2 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 775406	NM_001401501.2(MUC16):c.26006C>T (p.Thr8669Met)	MUC16 (T8629M +2 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 781385	NM_001401501.2(MUC16):c.24944C>T (p.Thr8315Met)	MUC16 (T8275M +2 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 780527	NM_001401501.2(MUC16):c.22653C>T (p.Ile7551=)	MUC16	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 775407	NM_001401501.2(MUC16):c.21434C>T (p.Thr7145Ile)	MUC16 (T7105I +2 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 726691	NM_001401501.2(MUC16):c.20548G>C (p.Ala6850Pro)	MUC16 (A6810P +2 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 726692	NM_001401501.2(MUC16):c.18263T>C (p.Met6088Thr)	MUC16 (M6048T +2 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 781386	NM_001401501.2(MUC16):c.18015G>A (p.Arg6005=)	MUC16	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 788376	NM_001401501.2(MUC16):c.17302T>G (p.Ser5768Ala)	MUC16 (S5728A +2 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 771925	NM_001401501.2(MUC16):c.17289G>T (p.Val5763=)	MUC16	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 771926	NM_001401501.2(MUC16):c.17136A>C (p.Thr5712=)	MUC16	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 781399	NM_001401501.2(MUC16):c.16846T>G (p.Ser5616Ala)	LOC126862848, MUC16 (S5576A +2 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 784828	NM_001401501.2(MUC16):c.16693T>C (p.Ser5565Pro)	LOC126862848, MUC16 (S5525P +2 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 781400	NM_001401501.2(MUC16):c.15297A>G (p.Leu5099=)	MUC16	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 781401	NM_001401501.2(MUC16):c.13888G>C (p.Asp4630His)	MUC16 (D4590H +2 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 724122	NM_001401501.2(MUC16):c.13679C>A (p.Ala4560Asp)	MUC16 (A4520D +2 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 780528	NM_001401501.2(MUC16):c.12801G>A (p.Glu4267=)	MUC16	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 780529	NM_001401501.2(MUC16):c.12609A>G (p.Val4203=)	MUC16	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 781402	NM_001401501.2(MUC16):c.9608C>T (p.Thr3203Met)	MUC16 (T3163M +2 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 781403	NM_001401501.2(MUC16):c.9549A>T (p.Thr3183=)	MUC16	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 781404	NM_001401501.2(MUC16):c.9421G>A (p.Ala3141Thr)	MUC16 (A3101T +2 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 781405	NM_001401501.2(MUC16):c.9387G>A (p.Glu3129=)	MUC16	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 781406	NM_001401501.2(MUC16):c.9285A>C (p.Leu3095=)	MUC16	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 781407	NM_001401501.2(MUC16):c.9084C>T (p.Ala3028=)	MUC16	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 781408	NM_001401501.2(MUC16):c.8621C>T (p.Thr2874Met)	MUC16 (T2834M +2 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 781409	NM_001401501.2(MUC16):c.8359G>A (p.Ala2787Thr)	MUC16 (A2747T +2 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 781410	NM_001401501.2(MUC16):c.8145G>A (p.Ser2715=)	MUC16	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 781411	NM_001401501.2(MUC16):c.7738A>C (p.Thr2580Pro)	MUC16 (T2540P +2 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 781412	NM_001401501.2(MUC16):c.7702G>A (p.Ala2568Thr)	MUC16 (A2528T +2 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 781413	NM_001401501.2(MUC16):c.7454G>A (p.Gly2485Asp)	MUC16 (G2445D +2 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 781414	NM_001401501.2(MUC16):c.7188C>G (p.Asp2396Glu)	MUC16 (D2356E +2 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 781427	NM_001401501.2(MUC16):c.7128A>G (p.Thr2376=)	MUC16	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 781428	NM_001401501.2(MUC16):c.6982G>T (p.Val2328Leu)	MUC16 (V2288L +2 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 781429	NM_001401501.2(MUC16):c.5875G>A (p.Ala1959Thr)	MUC16 (A1919T +2 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 781430	NM_001401501.2(MUC16):c.5871T>C (p.Pro1957=)	MUC16	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 781431	NM_001401501.2(MUC16):c.5754C>T (p.Gly1918=)	MUC16	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 781432	NM_001401501.2(MUC16):c.5666A>G (p.His1889Arg)	MUC16 (H1849R +2 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 781433	NM_001401501.2(MUC16):c.5402A>G (p.Glu1801Gly)	MUC16 (E1761G +2 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 781434	NM_001401501.2(MUC16):c.4461C>T (p.Pro1487=)	MUC16	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 781435	NM_001401501.2(MUC16):c.3885A>C (p.Ala1295=)	MUC16	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 781436	NM_001401501.2(MUC16):c.3241C>T (p.Pro1081Ser)	MUC16 (P1041S +2 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 781437	NM_001401501.2(MUC16):c.3214T>A (p.Ser1072Thr)	MUC16 (S1032T +2 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 781438	NM_001401501.2(MUC16):c.2263G>A (p.Ala755Thr)	MUC16 (A715T +2 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 780530	NM_001401501.2(MUC16):c.1970C>T (p.Thr657Ile)	MUC16 (T617I +2 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 781439	NM_001401501.2(MUC16):c.1173G>T (p.Gly391=)	MUC16	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 781440	NM_001401501.2(MUC16):c.302-139C>T	MUC16 (R15C)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign

ClinVar

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Items: 60