"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "CASP10" - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2940567	NM_032977.4(CASP10):c.13G>A (p.Gly5Ser)	CASP10 (G5S)	Single nucleotide variant (missense variant)	Autoimmune lymphoproliferative syndrome type 2A	GUncertain significance
Select item 333415	NM_032977.4(CASP10):c.20A>G (p.His7Arg)	CASP10 (H7R)	Single nucleotide variant (missense variant)	Autoimmune lymphoproliferative syndrome type 2A +1 more	GConflicting classifications of pathogenicity
Select item 1419109	NM_032977.4(CASP10):c.29C>G (p.Ser10Cys)	CASP10 (S10C)	Single nucleotide variant (missense variant)	Autoimmune lymphoproliferative syndrome type 2A	GUncertain significance
Select item 2921866	NM_032977.4(CASP10):c.45C>T (p.Asn15=)	CASP10	Single nucleotide variant (synonymous variant)	Autoimmune lymphoproliferative syndrome type 2A	GLikely benign
Select item 2942438	NM_032977.4(CASP10):c.47G>A (p.Cys16Tyr)	CASP10 (C16Y)	Single nucleotide variant (missense variant)	Autoimmune lymphoproliferative syndrome type 2A +1 more	GUncertain significance
Select item 333416	NM_032977.4(CASP10):c.49A>G (p.Lys17Glu)	CASP10 (K17E)	Single nucleotide variant (missense variant)	Autoimmune lymphoproliferative syndrome type 2A	GConflicting classifications of pathogenicity
Select item 2941340	NM_032977.4(CASP10):c.57C>G (p.Ser19Arg)	CASP10 (S19R)	Single nucleotide variant (missense variant)	Autoimmune lymphoproliferative syndrome type 2A	GUncertain significance
Select item 1356222	NM_032977.4(CASP10):c.61C>T (p.Arg21Cys)	CASP10 (R21C)	Single nucleotide variant (missense variant)	Autoimmune lymphoproliferative syndrome type 2A	GUncertain significance
Select item 1011666	NM_032977.4(CASP10):c.62G>A (p.Arg21His)	CASP10 (R21H)	Single nucleotide variant (missense variant)	not specified +2 more	GUncertain significance
Select item 2933753	NM_032977.4(CASP10):c.76A>G (p.Ile26Val)	CASP10 (I26V)	Single nucleotide variant (missense variant)	Autoimmune lymphoproliferative syndrome type 2A	GUncertain significance
Select item 714082	NM_032977.4(CASP10):c.81T>C (p.Ile27=)	CASP10	Single nucleotide variant (synonymous variant)	Autoimmune lymphoproliferative syndrome type 2A	GConflicting classifications of pathogenicity
Select item 1499880	NM_032977.4(CASP10):c.82G>C (p.Asp28His)	CASP10 (D28H)	Single nucleotide variant (missense variant)	Autoimmune lymphoproliferative syndrome type 2A	GUncertain significance
Select item 2946642	NM_032977.4(CASP10):c.86C>A (p.Ser29Ter)	CASP10 (S29*)	Single nucleotide variant (nonsense)	Autoimmune lymphoproliferative syndrome type 2A	GUncertain significance
Select item 1410685	NM_032977.4(CASP10):c.89A>T (p.Asn30Ile)	CASP10 (N30I)	Single nucleotide variant (missense variant)	Autoimmune lymphoproliferative syndrome type 2A	GUncertain significance
Select item 1576845	NM_032977.4(CASP10):c.90C>T (p.Asn30=)	CASP10	Single nucleotide variant (synonymous variant)	Autoimmune lymphoproliferative syndrome type 2A	GLikely benign
Select item 1378449	NM_032977.4(CASP10):c.94G>A (p.Gly32Arg)	CASP10 (G32R)	Single nucleotide variant (missense variant)	Autoimmune lymphoproliferative syndrome type 2A	GUncertain significance
Select item 2921782	NM_032977.4(CASP10):c.103G>A (p.Asp35Asn)	CASP10 (D35N)	Single nucleotide variant (missense variant)	Autoimmune lymphoproliferative syndrome type 2A	GUncertain significance
Select item 764073	NM_032977.4(CASP10):c.117C>T (p.Leu39=)	CASP10	Single nucleotide variant (synonymous variant)	Autoimmune lymphoproliferative syndrome type 2A	GLikely benign
Select item 1653611	NM_032977.4(CASP10):c.126C>T (p.Leu42=)	CASP10	Single nucleotide variant (synonymous variant)	Autoimmune lymphoproliferative syndrome type 2A	GLikely benign
Select item 1370585	NM_032977.4(CASP10):c.130A>T (p.Ile44Leu)	CASP10 (I44L)	Single nucleotide variant (missense variant)	Autoimmune lymphoproliferative syndrome type 2A	GUncertain significance
Select item 2923809	NM_032977.4(CASP10):c.134G>A (p.Gly45Glu)	CASP10 (G45E)	Single nucleotide variant (missense variant)	Autoimmune lymphoproliferative syndrome type 2A	GUncertain significance
Select item 854034	NM_032977.4(CASP10):c.136T>G (p.Leu46Val)	CASP10 (L46V)	Single nucleotide variant (missense variant)	Autoimmune lymphoproliferative syndrome type 2A	GUncertain significance
Select item 839357	NM_032977.4(CASP10):c.142C>T (p.Pro48Ser)	CASP10 (P48S)	Single nucleotide variant (missense variant)	Autoimmune lymphoproliferative syndrome type 2A	GUncertain significance
Select item 1108753	NM_032977.4(CASP10):c.144C>T (p.Pro48=)	CASP10	Single nucleotide variant (synonymous variant)	Autoimmune lymphoproliferative syndrome type 2A	GLikely benign
Select item 936365	NM_032977.4(CASP10):c.146A>G (p.Asn49Ser)	CASP10 (N49S)	Single nucleotide variant (missense variant)	Autoimmune lymphoproliferative syndrome type 2A	GUncertain significance
Select item 2936078	NM_032977.4(CASP10):c.153G>A (p.Lys51=)	CASP10	Single nucleotide variant (synonymous variant)	Autoimmune lymphoproliferative syndrome type 2A	GLikely benign
Select item 1353823	NM_032977.4(CASP10):c.163T>C (p.Ser55Pro)	CASP10 (S55P)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 757061	NM_032977.4(CASP10):c.174C>A (p.Ala58=)	CASP10	Single nucleotide variant (synonymous variant)	Autoimmune lymphoproliferative syndrome type 2A	GLikely benign
Select item 333417	NM_032977.4(CASP10):c.174C>T (p.Ala58=)	CASP10	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 592057	NM_032977.4(CASP10):c.176_177delinsGG (p.Ser59Trp)	CASP10 (S59W)	Indel (missense variant)	Autoimmune lymphoproliferative syndrome type 2A	GUncertain significance
Select item 333418	NM_032977.4(CASP10):c.177A>G (p.Ser59=)	CASP10	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign
Select item 644332	NM_032977.4(CASP10):c.199G>T (p.Ala67Ser)	CASP10 (A67S)	Single nucleotide variant (missense variant)	Autoimmune lymphoproliferative syndrome type 2A	GUncertain significance
Select item 838561	NM_032977.4(CASP10):c.208C>G (p.Leu70Val)	CASP10 (L70V)	Single nucleotide variant (missense variant)	Autoimmune lymphoproliferative syndrome type 2A	GUncertain significance
Select item 1998052	NM_032977.4(CASP10):c.211C>T (p.Leu71=)	CASP10	Single nucleotide variant (synonymous variant)	Autoimmune lymphoproliferative syndrome type 2A	GLikely benign
Select item 1345901	NM_032977.4(CASP10):c.215G>C (p.Ser72Thr)	CASP10 (S72T)	Single nucleotide variant (missense variant)	Autoimmune lymphoproliferative syndrome type 2A	GUncertain significance
Select item 2951142	NM_032977.4(CASP10):c.225C>T (p.Asp75=)	CASP10	Single nucleotide variant (synonymous variant)	Autoimmune lymphoproliferative syndrome type 2A	GLikely benign
Select item 577661	NM_032977.4(CASP10):c.226C>A (p.Pro76Thr)	CASP10 (P76T)	Single nucleotide variant (missense variant)	Autoimmune lymphoproliferative syndrome type 2A	GUncertain significance
Select item 1638647	NM_032977.4(CASP10):c.234C>T (p.Phe78=)	CASP10	Single nucleotide variant (synonymous variant)	Autoimmune lymphoproliferative syndrome type 2A	GLikely benign
Select item 1039059	NM_032977.4(CASP10):c.244CTC[1] (p.Leu83del)	CASP10 (L83del)	Microsatellite (inframe_deletion)	Autoimmune lymphoproliferative syndrome type 2A	GUncertain significance
Select item 2926700	NM_032977.4(CASP10):c.247C>T (p.Leu83Phe)	CASP10 (L83F)	Single nucleotide variant (missense variant)	Autoimmune lymphoproliferative syndrome type 2A	GUncertain significance
Select item 535759	NM_032977.4(CASP10):c.247C>G (p.Leu83Val)	CASP10 (L83V)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2926874	NM_032977.4(CASP10):c.248T>C (p.Leu83Pro)	CASP10 (L83P)	Single nucleotide variant (missense variant)	Autoimmune lymphoproliferative syndrome type 2A	GUncertain significance
Select item 2130917	NM_032977.4(CASP10):c.249C>T (p.Leu83=)	CASP10	Single nucleotide variant (synonymous variant)	Autoimmune lymphoproliferative syndrome type 2A	GLikely benign
Select item 1365892	NM_032977.4(CASP10):c.250T>C (p.Tyr84His)	CASP10 (Y84H)	Single nucleotide variant (missense variant)	Autoimmune lymphoproliferative syndrome type 2A	GUncertain significance
Select item 1997473	NM_032977.4(CASP10):c.251A>G (p.Tyr84Cys)	CASP10 (Y84C)	Single nucleotide variant (missense variant)	Autoimmune lymphoproliferative syndrome type 2A	GUncertain significance
Select item 1014752	NM_032977.4(CASP10):c.258A>G (p.Ile86Met)	CASP10 (I86M)	Single nucleotide variant (missense variant)	Autoimmune lymphoproliferative syndrome type 2A	GUncertain significance
Select item 569038	NM_032977.4(CASP10):c.259C>T (p.Arg87Trp)	CASP10 (R87W)	Single nucleotide variant (missense variant)	not provided +3 more	GUncertain significance
Select item 1997153	NM_032977.4(CASP10):c.260G>A (p.Arg87Gln)	CASP10 (R87Q)	Single nucleotide variant (missense variant)	Autoimmune lymphoproliferative syndrome type 2A	GUncertain significance
Select item 2944963	NM_032977.4(CASP10):c.270G>A (p.Lys90=)	CASP10	Single nucleotide variant (synonymous variant)	Autoimmune lymphoproliferative syndrome type 2A	GLikely benign
Select item 1103035	NM_032977.4(CASP10):c.271C>T (p.Leu91=)	CASP10	Single nucleotide variant (synonymous variant)	Autoimmune lymphoproliferative syndrome type 2A	GLikely benign
Select item 2939561	NM_032977.4(CASP10):c.278A>C (p.Gln93Pro)	CASP10 (Q93P)	Single nucleotide variant (missense variant)	Autoimmune lymphoproliferative syndrome type 2A	GUncertain significance
Select item 1052960	NM_032977.4(CASP10):c.284T>C (p.Leu95Pro)	CASP10 (L95P)	Single nucleotide variant (missense variant)	Autoimmune lymphoproliferative syndrome type 2A	GUncertain significance
Select item 785750	NM_032977.4(CASP10):c.295A>G (p.Lys99Glu)	CASP10 (K99E)	Single nucleotide variant (missense variant)	Autoimmune lymphoproliferative syndrome type 2A	GLikely benign
Select item 1976325	NM_032977.4(CASP10):c.303A>T (p.Glu101Asp)	CASP10 (E101D)	Single nucleotide variant (missense variant)	Autoimmune lymphoproliferative syndrome type 2A	GUncertain significance
Select item 2135216	NM_032977.4(CASP10):c.309G>A (p.Glu103=)	CASP10	Single nucleotide variant (synonymous variant)	Autoimmune lymphoproliferative syndrome type 2A	GLikely benign
Select item 571302	NM_032977.4(CASP10):c.310C>T (p.Arg104Ter)	CASP10 (R104*)	Single nucleotide variant (nonsense)	Autoimmune lymphoproliferative syndrome type 2A	GUncertain significance
Select item 1057464	NM_032977.4(CASP10):c.311G>A (p.Arg104Gln)	CASP10 (R104Q)	Single nucleotide variant (missense variant)	Autoimmune lymphoproliferative syndrome type 2A +1 more	GUncertain significance
Select item 1976326	NM_032977.4(CASP10):c.314T>A (p.Leu105Gln)	CASP10 (L105Q)	Single nucleotide variant (missense variant)	Autoimmune lymphoproliferative syndrome type 2A	GUncertain significance
Select item 1436583	NM_032977.4(CASP10):c.314T>C (p.Leu105Pro)	CASP10 (L105P)	Single nucleotide variant (missense variant)	Autoimmune lymphoproliferative syndrome type 2A	GUncertain significance
Select item 801852	NM_032977.4(CASP10):c.325C>T (p.Arg109Ter)	CASP10 (R109*)	Single nucleotide variant (nonsense)	Autoimmune lymphoproliferative syndrome type 1 +1 more	GUncertain significance
Select item 2162939	NM_032977.4(CASP10):c.326G>C (p.Arg109Pro)	CASP10 (R109P)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 1351812	NM_032977.4(CASP10):c.332G>C (p.Arg111Thr)	CASP10 (R111T)	Single nucleotide variant (missense variant)	Autoimmune lymphoproliferative syndrome type 2A	GUncertain significance
Select item 1386864	NM_032977.4(CASP10):c.335T>C (p.Val112Ala)	CASP10 (V112A)	Single nucleotide variant (missense variant)	Autoimmune lymphoproliferative syndrome type 2A +1 more	GUncertain significance
Select item 1301792	NM_032977.4(CASP10):c.347+2T>G	CASP10	Single nucleotide variant (splice donor variant)	Autoimmune lymphoproliferative syndrome type 2A +1 more	GUncertain significance
Select item 2923490	NM_032977.4(CASP10):c.347+6G>A	CASP10	Single nucleotide variant (intron variant)	Autoimmune lymphoproliferative syndrome type 2A	GUncertain significance
Select item 333419	NM_032977.4(CASP10):c.347+8C>T	CASP10	Single nucleotide variant (intron variant)	Autoimmune lymphoproliferative syndrome type 2A +1 more	GBenign/Likely benign
Select item 1081682	NM_032977.4(CASP10):c.347+9G>A	CASP10	Single nucleotide variant (intron variant)	Autoimmune lymphoproliferative syndrome type 2A	GLikely benign
Select item 333420	NM_032977.4(CASP10):c.347+9G>T	CASP10	Single nucleotide variant (intron variant)	Autoimmune lymphoproliferative syndrome type 2A +1 more	GBenign
Select item 535762	NM_032977.4(CASP10):c.347+10G>T	CASP10	Single nucleotide variant (intron variant)	Autoimmune lymphoproliferative syndrome type 2A	GLikely benign
Select item 2117089	NM_032977.4(CASP10):c.347+11G>A	CASP10	Single nucleotide variant (intron variant)	Autoimmune lymphoproliferative syndrome type 2A	GLikely benign
Select item 2082117	NM_032977.4(CASP10):c.347+16T>C	CASP10	Single nucleotide variant (intron variant)	Autoimmune lymphoproliferative syndrome type 2A	GLikely benign
Select item 1624663	NM_032977.4(CASP10):c.348-16dup	CASP10	Duplication (intron variant)	Autoimmune lymphoproliferative syndrome type 2A	GBenign
Select item 2933385	NM_032977.4(CASP10):c.348-13G>C	CASP10	Single nucleotide variant (intron variant)	Autoimmune lymphoproliferative syndrome type 2A	GLikely benign
Select item 766739	NM_032977.4(CASP10):c.348-4T>C	CASP10	Single nucleotide variant (intron variant)	Autoimmune lymphoproliferative syndrome type 2A	GLikely benign
Select item 1130143	NM_032977.4(CASP10):c.360C>T (p.Tyr120=)	CASP10	Single nucleotide variant (synonymous variant)	Autoimmune lymphoproliferative syndrome type 2A	GLikely benign
Select item 333421	NM_032977.4(CASP10):c.361G>A (p.Glu121Lys)	CASP10 (E121K)	Single nucleotide variant (missense variant)	Autoimmune lymphoproliferative syndrome type 2A	GUncertain significance
Select item 965519	NM_032977.4(CASP10):c.365T>C (p.Leu122Pro)	CASP10 (L122P)	Single nucleotide variant (missense variant)	Autoimmune lymphoproliferative syndrome type 2A	GUncertain significance
Select item 1447584	NM_032977.4(CASP10):c.376A>G (p.Ile126Val)	CASP10 (I126V)	Single nucleotide variant (missense variant)	Autoimmune lymphoproliferative syndrome type 2A	GUncertain significance
Select item 2418856	NM_032977.4(CASP10):c.387_388del (p.Asn130fs)	CASP10 (N130fs)	Microsatellite (frameshift variant)	Autoimmune lymphoproliferative syndrome type 2A	GUncertain significance
Select item 1063707	NM_032977.4(CASP10):c.385G>A (p.Glu129Lys)	CASP10 (E129K)	Single nucleotide variant (missense variant)	Autoimmune lymphoproliferative syndrome type 2A	GUncertain significance
Select item 2939442	NM_032977.4(CASP10):c.387G>C (p.Glu129Asp)	CASP10 (E129D)	Single nucleotide variant (missense variant)	Autoimmune lymphoproliferative syndrome type 2A	GUncertain significance
Select item 2930300	NM_032977.4(CASP10):c.387G>T (p.Glu129Asp)	CASP10 (E129D)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 968381	NM_032977.4(CASP10):c.389_393delinsC (p.Asn130fs)	CASP10 (N130fs)	Indel (frameshift variant)	Autoimmune lymphoproliferative syndrome type 2A	GUncertain significance
Select item 1529368	NM_032977.4(CASP10):c.390C>T (p.Asn130=)	CASP10	Single nucleotide variant (synonymous variant)	Autoimmune lymphoproliferative syndrome type 2A	GLikely benign
Select item 1477607	NM_032977.4(CASP10):c.396G>C (p.Lys132Asn)	CASP10 (K132N)	Single nucleotide variant (missense variant)	Autoimmune lymphoproliferative syndrome type 2A	GUncertain significance
Select item 1137523	NM_032977.4(CASP10):c.405C>A (p.Ile135=)	CASP10	Single nucleotide variant (synonymous variant)	Autoimmune lymphoproliferative syndrome type 2A	GLikely benign
Select item 659317	NM_032977.4(CASP10):c.413T>C (p.Leu138Pro)	CASP10 (L138P)	Single nucleotide variant (missense variant)	Autoimmune lymphoproliferative syndrome type 2A	GUncertain significance
Select item 2104193	NM_032977.4(CASP10):c.416A>C (p.Lys139Thr)	CASP10 (K139T)	Single nucleotide variant (missense variant)	Autoimmune lymphoproliferative syndrome type 2A	GUncertain significance
Select item 2103603	NM_032977.4(CASP10):c.419A>C (p.Asp140Ala)	CASP10 (D140A)	Single nucleotide variant (missense variant)	Autoimmune lymphoproliferative syndrome type 2A	GUncertain significance
Select item 1460718	NM_032977.4(CASP10):c.422C>T (p.Ser141Leu)	CASP10 (S141L)	Single nucleotide variant (missense variant)	Autoimmune lymphoproliferative syndrome type 2A	GUncertain significance
Select item 1136664	NM_032977.4(CASP10):c.423G>T (p.Ser141=)	CASP10	Single nucleotide variant (synonymous variant)	Autoimmune lymphoproliferative syndrome type 2A	GLikely benign
Select item 1113561	NM_032977.4(CASP10):c.423G>A (p.Ser141=)	CASP10	Single nucleotide variant (synonymous variant)	Autoimmune lymphoproliferative syndrome type 2A	GLikely benign
Select item 7768	NM_032977.4(CASP10):c.440T>C (p.Met147Thr)	CASP10 (M147T)	Single nucleotide variant (missense variant)	Autoimmune lymphoproliferative syndrome type 2A +1 more	GUncertain significance
Select item 2948343	NM_032977.4(CASP10):c.441G>A (p.Met147Ile)	CASP10 (M147I)	Single nucleotide variant (missense variant)	Autoimmune lymphoproliferative syndrome type 2A	GUncertain significance
Select item 2943292	NM_032977.4(CASP10):c.441+8G>A	CASP10	Single nucleotide variant (intron variant)	Autoimmune lymphoproliferative syndrome type 2A	GLikely benign
Select item 2052188	NM_032977.4(CASP10):c.441+19A>G	CASP10	Single nucleotide variant (intron variant)	Autoimmune lymphoproliferative syndrome type 2A	GUncertain significance
Select item 1477118	NM_032977.4(CASP10):c.442-20C>G	CASP10	Single nucleotide variant (intron variant)	Autoimmune lymphoproliferative syndrome type 2A	GLikely benign
Select item 2943093	NM_032977.4(CASP10):c.442-18C>G	CASP10	Single nucleotide variant (intron variant)	Autoimmune lymphoproliferative syndrome type 2A	GLikely benign
Select item 895421	NM_032977.4(CASP10):c.442-14T>G	CASP10	Single nucleotide variant (intron variant)	Autoimmune lymphoproliferative syndrome type 2A	GConflicting classifications of pathogenicity
Select item 2942108	NM_032977.4(CASP10):c.448C>A (p.Leu150Ile)	CASP10 (L150I)	Single nucleotide variant (missense variant)	Autoimmune lymphoproliferative syndrome type 2A	GUncertain significance

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