"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "LOC1300 - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 596138	NM_003977.4(AIP):c.100-18C>T	AIP, LOC130006206	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 1658411	NM_003977.4(AIP):c.100-17T>G	AIP, LOC130006206	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1658276	NM_003977.4(AIP):c.100-16C>T	AIP, LOC130006206	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2822775	NM_003977.4(AIP):c.100-15G>C	LOC130006206, AIP	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1590790	NM_003977.4(AIP):c.100-15G>A	AIP, LOC130006206	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1637587	NM_003977.4(AIP):c.100-13A>T	AIP, LOC130006206	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1536895	NM_003977.4(AIP):c.100-13A>G	AIP, LOC130006206	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1394471	NM_003977.4(AIP):c.100-12T>G	AIP, LOC130006206	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 1153003	NM_003977.4(AIP):c.100-7C>T	AIP, LOC130006206	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2996240	NM_003977.4(AIP):c.100-6C>T	AIP, LOC130006206	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1169842	NM_003977.4(AIP):c.100-6C>A	AIP, LOC130006206	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome +2 more	GBenign
Select item 2954776	NM_003977.4(AIP):c.100-5C>T	AIP, LOC130006206	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 1536395	NM_003977.4(AIP):c.100-4A>C	AIP, LOC130006206	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1470153	NM_003977.4(AIP):c.100-4del	AIP, LOC130006206	Deletion (intron variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2419610	NM_003977.4(AIP):c.100-3C>G	AIP, LOC130006206	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 822003	NM_003977.4(AIP):c.100G>T (p.Ala34Ser)	AIP, LOC130006206 (A34S)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 485058	NM_003977.4(AIP):c.104C>T (p.Thr35Met)	AIP, LOC130006206 (T35M)	Single nucleotide variant (5 prime UTR variant +1 more)	Somatotroph adenoma +2 more	GUncertain significance
Select item 1673800	NM_003977.4(AIP):c.105G>T (p.Thr35=)	AIP, LOC130006206	Single nucleotide variant (5 prime UTR variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 818316	NM_003977.4(AIP):c.105G>A (p.Thr35=)	AIP, LOC130006206	Single nucleotide variant (5 prime UTR variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 822137	NM_003977.4(AIP):c.108C>T (p.Phe36=)	AIP, LOC130006206	Single nucleotide variant (5 prime UTR variant +1 more)	not provided +1 more	GLikely benign
Select item 2127517	NM_003977.4(AIP):c.109C>T (p.His37Tyr)	AIP, LOC130006206 (H37Y)	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GUncertain significance
Select item 1728034	NM_003977.4(AIP):c.112T>C (p.Tyr38His)	AIP, LOC130006206 (Y38H)	Single nucleotide variant (5 prime UTR variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 1001466	NM_003977.4(AIP):c.115C>G (p.Arg39Gly)	AIP, LOC130006206 (R39G)	Single nucleotide variant (5 prime UTR variant +1 more)	not provided +1 more	GUncertain significance
Select item 861039	NM_003977.4(AIP):c.115C>T (p.Arg39Trp)	AIP, LOC130006206 (R39W)	Single nucleotide variant (5 prime UTR variant +1 more)	Somatotroph adenoma +2 more	GUncertain significance
Select item 818481	NM_003977.4(AIP):c.116G>A (p.Arg39Gln)	LOC130006206, AIP (R39Q)	Single nucleotide variant (5 prime UTR variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 818567	NM_003977.4(AIP):c.119C>T (p.Thr40Met)	AIP, LOC130006206 (T40M)	Single nucleotide variant (5 prime UTR variant +1 more)	not provided +1 more	GUncertain significance
Select item 818603	NM_003977.4(AIP):c.120G>A (p.Thr40=)	AIP, LOC130006206	Single nucleotide variant (5 prime UTR variant +1 more)	not provided +1 more	GLikely benign
Select item 2856094	NM_003977.4(AIP):c.121C>G (p.Leu41Val)	AIP, LOC130006206 (L41V)	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GUncertain significance
Select item 1543340	NM_003977.4(AIP):c.123G>A (p.Leu41=)	AIP, LOC130006206	Single nucleotide variant (5 prime UTR variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 1493680	NM_003977.4(AIP):c.126C>G (p.His42Gln)	AIP, LOC130006206 (H42Q)	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GUncertain significance
Select item 1127735	NM_003977.4(AIP):c.126C>T (p.His42=)	AIP, LOC130006206	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GLikely benign
Select item 2087473	NM_003977.4(AIP):c.127A>G (p.Ser43Gly)	AIP, LOC130006206 (S43G)	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GUncertain significance
Select item 259204	NM_003977.4(AIP):c.132C>T (p.Asp44=)	AIP, LOC130006206	Single nucleotide variant (5 prime UTR variant +1 more)	not specified +3 more	GBenign
Select item 1040600	NM_003977.4(AIP):c.133G>A (p.Asp45Asn)	AIP, LOC130006206 (D45N)	Single nucleotide variant (5 prime UTR variant +1 more)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 1770561	NM_003977.4(AIP):c.134A>T (p.Asp45Val)	AIP, LOC130006206 (D45V)	Single nucleotide variant (5 prime UTR variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 2102813	NM_003977.4(AIP):c.135C>G (p.Asp45Glu)	AIP, LOC130006206 (D45E)	Single nucleotide variant (5 prime UTR variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 41162	NM_003977.4(AIP):c.135C>T (p.Asp45=)	AIP, LOC130006206	Single nucleotide variant (5 prime UTR variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 1516920	NM_003977.4(AIP):c.136G>C (p.Glu46Gln)	AIP, LOC130006206 (E46Q)	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GUncertain significance
Select item 819007	NM_003977.4(AIP):c.136G>A (p.Glu46Lys)	AIP, LOC130006206 (E46K)	Single nucleotide variant (5 prime UTR variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 1463124	NM_003977.4(AIP):c.138G>T (p.Glu46Asp)	AIP, LOC130006206 (E46D)	Single nucleotide variant (5 prime UTR variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 41163	NM_003977.4(AIP):c.140_163del (p.Gly47_Arg54del)	AIP, LOC130006206	Deletion (5 prime UTR variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 819117	NM_003977.4(AIP):c.139G>A (p.Gly47Ser)	AIP, LOC130006206 (G47S)	Single nucleotide variant (5 prime UTR variant +1 more)	not provided +2 more	GUncertain significance
Select item 1430344	NM_003977.4(AIP):c.140G>A (p.Gly47Asp)	AIP, LOC130006206 (G47D)	Single nucleotide variant (5 prime UTR variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 2823790	NM_003977.4(AIP):c.141C>T (p.Gly47=)	LOC130006206, AIP	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GLikely benign
Select item 1620193	NM_003977.4(AIP):c.144C>G (p.Thr48=)	AIP, LOC130006206	Single nucleotide variant (5 prime UTR variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 819248	NM_003977.4(AIP):c.144C>T (p.Thr48=)	AIP, LOC130006206	Single nucleotide variant (5 prime UTR variant +1 more)	Somatotroph adenoma +2 more	GBenign/Likely benign
Select item 1516459	NM_003977.4(AIP):c.145G>T (p.Val49Leu)	AIP, LOC130006206 (V49L)	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GUncertain significance
Select item 41164	NM_003977.4(AIP):c.145G>A (p.Val49Met)	AIP, LOC130006206 (V49M)	Single nucleotide variant (5 prime UTR variant +1 more)	Somatotroph adenoma +2 more	GConflicting classifications of pathogenicity
Select item 819423	NM_003977.4(AIP):c.151G>A (p.Asp51Asn)	AIP, LOC130006206 (D51N)	Single nucleotide variant (5 prime UTR variant +1 more)	not provided +2 more	GUncertain significance
Select item 2010264	NM_003977.4(AIP):c.152A>G (p.Asp51Gly)	AIP, LOC130006206 (D51G)	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GUncertain significance
Select item 1470776	NM_003977.4(AIP):c.152A>T (p.Asp51Val)	AIP, LOC130006206 (D51V)	Single nucleotide variant (5 prime UTR variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 819440	NM_003977.4(AIP):c.153C>T (p.Asp51=)	AIP, LOC130006206	Single nucleotide variant (5 prime UTR variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 1775024	NM_003977.4(AIP):c.154G>A (p.Asp52Asn)	AIP, LOC130006206 (D52N)	Single nucleotide variant (5 prime UTR variant +1 more)	not provided +1 more	GUncertain significance
Select item 1500478	NM_003977.4(AIP):c.155A>G (p.Asp52Gly)	AIP, LOC130006206 (D52G)	Single nucleotide variant (5 prime UTR variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 819642	NM_003977.4(AIP):c.159C>T (p.Ser53=)	AIP, LOC130006206	Single nucleotide variant (5 prime UTR variant +1 more)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 819659	NM_003977.4(AIP):c.160C>T (p.Arg54Trp)	AIP, LOC130006206 (R54W)	Single nucleotide variant (5 prime UTR variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 819687	NM_003977.4(AIP):c.161G>A (p.Arg54Gln)	AIP, LOC130006206 (R54Q)	Single nucleotide variant (5 prime UTR variant +1 more)	not provided +2 more	GUncertain significance
Select item 1777021	NM_003977.4(AIP):c.163G>T (p.Ala55Ser)	AIP, LOC130006206 (A55S)	Single nucleotide variant (5 prime UTR variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 1023228	NM_003977.4(AIP):c.163G>A (p.Ala55Thr)	AIP, LOC130006206 (A55T)	Single nucleotide variant (5 prime UTR variant +1 more)	not provided +1 more	GUncertain significance
Select item 1022659	NM_003977.4(AIP):c.164C>T (p.Ala55Val)	AIP, LOC130006206 (A55V)	Single nucleotide variant (5 prime UTR variant +1 more)	Somatotroph adenoma +2 more	GConflicting classifications of pathogenicity
Select item 877266	NM_003977.4(AIP):c.166C>T (p.Arg56Cys)	AIP, LOC130006206 (R56C)	Single nucleotide variant (5 prime UTR variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 1777879	NM_003977.4(AIP):c.167G>C (p.Arg56Pro)	AIP, LOC130006206 (R56P)	Single nucleotide variant (5 prime UTR variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 964401	NM_003977.4(AIP):c.167G>A (p.Arg56His)	AIP, LOC130006206 (R56H)	Single nucleotide variant (5 prime UTR variant +1 more)	not provided +1 more	GUncertain significance
Select item 1035289	NM_003977.4(AIP):c.169G>A (p.Gly57Ser)	AIP, LOC130006206 (G57S)	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GUncertain significance
Select item 1376671	NM_003977.4(AIP):c.170G>A (p.Gly57Asp)	AIP, LOC130006206 (G57D)	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GUncertain significance
Select item 2897012	NM_003977.4(AIP):c.171C>G (p.Gly57=)	AIP, LOC130006206	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GLikely benign
Select item 2834365	NM_003977.4(AIP):c.173A>G (p.Lys58Arg)	AIP, LOC130006206 (K58R)	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GUncertain significance
Select item 1375499	NM_003977.4(AIP):c.174G>T (p.Lys58Asn)	AIP, LOC130006206 (K58N)	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GUncertain significance
Select item 1078767	NM_003977.4(AIP):c.174G>A (p.Lys58=)	AIP, LOC130006206	Single nucleotide variant (5 prime UTR variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 41166	NM_003977.4(AIP):c.174G>C (p.Lys58Asn)	AIP, LOC130006206 (K58N)	Single nucleotide variant (5 prime UTR variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 859123	NM_003977.4(AIP):c.175C>T (p.Pro59Ser)	AIP, LOC130006206 (P59S)	Single nucleotide variant (5 prime UTR variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 1508933	NM_003977.4(AIP):c.178A>G (p.Met60Val)	AIP, LOC130006206 (M60V +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 1005479	NM_003977.4(AIP):c.182A>G (p.Glu61Gly)	AIP, LOC130006206 (E2G +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 1135824	NM_003977.4(AIP):c.183G>A (p.Glu61=)	AIP, LOC130006206	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1717420	NM_003977.4(AIP):c.184C>T (p.Leu62Phe)	AIP, LOC130006206 (L3F +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1781656	NM_003977.4(AIP):c.186C>T (p.Leu62=)	AIP, LOC130006206	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1000149	NM_003977.4(AIP):c.188T>A (p.Ile63Asn)	AIP, LOC130006206 (I4N +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2102628	NM_003977.4(AIP):c.189C>A (p.Ile63=)	AIP, LOC130006206	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 2105815	NM_003977.4(AIP):c.192T>G (p.Ile64Met)	AIP, LOC130006206 (I64M +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1079361	NM_003977.4(AIP):c.192T>C (p.Ile64=)	AIP, LOC130006206	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1461191	NM_003977.4(AIP):c.194G>A (p.Gly65Asp)	AIP, LOC130006206 (G6D +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1093540	NM_003977.4(AIP):c.198G>A (p.Lys66=)	AIP, LOC130006206	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 2833367	NM_003977.4(AIP):c.201G>A (p.Lys67=)	AIP, LOC130006206	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2769664	NM_003977.4(AIP):c.204C>G (p.Phe68Leu)	AIP, LOC130006206 (F68L +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 820621	NM_003977.4(AIP):c.205A>G (p.Lys69Glu)	AIP, LOC130006206 (K69E +1 more)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 1715305	NM_003977.4(AIP):c.206A>C (p.Lys69Thr)	AIP, LOC130006206 (K10T +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2008182	NM_003977.4(AIP):c.208C>G (p.Leu70Val)	AIP, LOC130006206 (L70V +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1612490	NM_003977.4(AIP):c.213T>G (p.Pro71=)	AIP, LOC130006206	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 1439844	NM_003977.4(AIP):c.214G>A (p.Val72Met)	AIP, LOC130006206 (V13M +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1360852	NM_003977.4(AIP):c.214G>C (p.Val72Leu)	AIP, LOC130006206 (V13L +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GConflicting classifications of pathogenicity
Select item 1153856	NM_003977.4(AIP):c.222G>A (p.Glu74=)	AIP, LOC130006206	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 2120028	NM_003977.4(AIP):c.225C>G (p.Thr75=)	LOC130006206, AIP	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 387905	NM_003977.4(AIP):c.226A>G (p.Ile76Val)	AIP, LOC130006206 (I76V +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 1084640	NM_003977.4(AIP):c.228C>T (p.Ile76=)	AIP, LOC130006206	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 821052	NM_003977.4(AIP):c.229G>C (p.Val77Leu)	LOC130006206, AIP (V18L +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 821051	NM_003977.4(AIP):c.229G>A (p.Val77Met)	AIP, LOC130006206 (V77M +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 1153515	NM_003977.4(AIP):c.234C>T (p.Cys78=)	AIP, LOC130006206	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1719855	NM_003977.4(AIP):c.235A>G (p.Thr79Ala)	AIP, LOC130006206 (T20A +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 1790270	NM_003977.4(AIP):c.236C>T (p.Thr79Ile)	AIP, LOC130006206 (T20I +1 more)	Single nucleotide variant (missense variant)	Somatotroph adenoma +2 more	GUncertain significance
Select item 1064219	NM_003977.4(AIP):c.236C>A (p.Thr79Asn)	AIP, LOC130006206 (T20N +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance

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