ClinVar (all) for Orgtrack (Select 505998) - ClinVar - NCBI

Warning: The NCBI web site requires JavaScript to function. more...

Links from Orgtrack

Items: 1 to 100 of 1000

<< First< Prev

Page of 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 983210	NM_001114753.3(ENG):c.503TCC[4] (p.Leu170_Arg171insLeu)	ENG	Microsatellite (inframe_insertion +2 more)	Telangiectasia, hereditary hemorrhagic, type 1	GLikely pathogenic
Select item 983209	NM_001114753.3(ENG):c.496del (p.Gln166fs)	ENG (Q166fs)	Deletion (frameshift variant +1 more)	Telangiectasia, hereditary hemorrhagic, type 1	GPathogenic
Select item 983208	NM_001114753.3(ENG):c.39del (p.Leu14fs)	ENG (L14fs)	Deletion (frameshift variant)	Telangiectasia, hereditary hemorrhagic, type 1	GPathogenic
Select item 983207	NM_001114753.3(ENG):c.967_968del (p.Val323fs)	ENG (V141fs +1 more)	Deletion (frameshift variant)	Telangiectasia, hereditary hemorrhagic, type 1	GPathogenic
Select item 983206	NM_001114753.3(ENG):c.923C>A (p.Ala308Asp)	ENG (A126D +1 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +2 more	GPathogenic/Likely pathogenic
Select item 983205	NM_001114753.3(ENG):c.620G>A (p.Cys207Tyr)	ENG (C207Y +1 more)	Single nucleotide variant (missense variant)	Telangiectasia, hereditary hemorrhagic, type 1	GLikely pathogenic
Select item 983204	NM_001114753.3(ENG):c.496dup (p.Gln166fs)	ENG (Q166fs)	Duplication (frameshift variant +1 more)	not provided +3 more	GPathogenic
Select item 983203	NM_001114753.3(ENG):c.370del (p.Leu124fs)	ENG (L124fs)	Deletion (frameshift variant +1 more)	Telangiectasia, hereditary hemorrhagic, type 1	GPathogenic
Select item 983202	NM_001114753.3(ENG):c.328C>T (p.Gln110Ter)	ENG (Q110*)	Single nucleotide variant (nonsense +1 more)	Telangiectasia, hereditary hemorrhagic, type 1 +1 more	GPathogenic
Select item 983201	NM_001114753.3(ENG):c.1484T>C (p.Leu495Pro)	ENG, LOC102723566 (L313P +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Telangiectasia, hereditary hemorrhagic, type 1	GLikely pathogenic
Select item 983200	NM_001114753.3(ENG):c.146del (p.Val49fs)	ENG (V49fs)	Deletion (frameshift variant +1 more)	Telangiectasia, hereditary hemorrhagic, type 1	GPathogenic
Select item 983199	NM_001114753.3(ENG):c.1437_1456dup (p.Phe486fs)	ENG, LOC102723566 (F304fs +1 more)	Duplication (frameshift variant +1 more)	Telangiectasia, hereditary hemorrhagic, type 1	GPathogenic
Select item 983198	NM_001114753.3(ENG):c.1411C>T (p.Gln471Ter)	ENG, LOC102723566 (Q289* +1 more)	Single nucleotide variant (nonsense)	Telangiectasia, hereditary hemorrhagic, type 1 +2 more	GPathogenic
Select item 983197	NM_001114753.3(ENG):c.1384C>T (p.Gln462Ter)	LOC102723566, ENG (Q280* +1 more)	Single nucleotide variant (nonsense)	Telangiectasia, hereditary hemorrhagic, type 1	GPathogenic
Select item 983196	NM_001114753.3(ENG):c.1365C>A (p.Tyr455Ter)	ENG, LOC102723566 (Y273* +1 more)	Single nucleotide variant (nonsense)	not provided +2 more	GPathogenic
Select item 983195	NM_001114753.3(ENG):c.1311+5G>C	ENG, LOC102723566	Single nucleotide variant (intron variant)	Telangiectasia, hereditary hemorrhagic, type 1	GLikely pathogenic
Select item 983194	NM_001114753.3(ENG):c.1337A>G (p.Asp446Gly)	ENG, LOC102723566 (D264G +1 more)	Single nucleotide variant (missense variant)	Telangiectasia, hereditary hemorrhagic, type 1	GLikely benign
Select item 982496	NM_001114753.3(ENG):c.1273-2A>T	ENG, LOC102723566	Single nucleotide variant (splice acceptor variant)	Telangiectasia, hereditary hemorrhagic, type 1	GPathogenic
Select item 982495	NM_001114753.3(ENG):c.1268A>G (p.Asn423Ser)	ENG, LOC102723566 (N241S +1 more)	Single nucleotide variant (missense variant)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 982494	NM_001114753.3(ENG):c.1238G>A (p.Gly413Asp)	ENG, LOC102723566 (G231D +1 more)	Single nucleotide variant (missense variant)	Telangiectasia, hereditary hemorrhagic, type 1	GLikely benign
Select item 982493	NM_001114753.3(ENG):c.1183G>T (p.Glu395Ter)	ENG, LOC102723566 (E213* +1 more)	Single nucleotide variant (nonsense)	Telangiectasia, hereditary hemorrhagic, type 1	GPathogenic
Select item 982492	NM_016204.4(GDF2):c.348T>C (p.Asp116=)	GDF2	Single nucleotide variant (synonymous variant)	Telangiectasia, hereditary hemorrhagic, type 5	GUncertain significance
Select item 982491	NM_000020.3(ACVRL1):c.948G>C (p.Glu316Asp)	ACVRL1 (E316D)	Single nucleotide variant (missense variant)	Telangiectasia, hereditary hemorrhagic, type 2	GConflicting classifications of pathogenicity
Select item 982490	NM_000020.3(ACVRL1):c.916_917insTCA (p.Ala306delinsValThr)	ACVRL1	Insertion (inframe_indel)	Telangiectasia, hereditary hemorrhagic, type 2	GLikely pathogenic
Select item 982489	NM_000020.3(ACVRL1):c.848G>T (p.Gly283Val)	ACVRL1 (G283V)	Single nucleotide variant (missense variant)	Telangiectasia, hereditary hemorrhagic, type 2	GLikely pathogenic
Select item 982488	NM_000020.3(ACVRL1):c.830C>G (p.Thr277Arg)	ACVRL1 (T277R)	Single nucleotide variant (missense variant)	Telangiectasia, hereditary hemorrhagic, type 2	GPathogenic/Likely pathogenic
Select item 982487	NM_000020.3(ACVRL1):c.626-2A>G	ACVRL1	Single nucleotide variant (splice acceptor variant)	Telangiectasia, hereditary hemorrhagic, type 2	GPathogenic
Select item 982486	NM_000020.3(ACVRL1):c.475G>T (p.Glu159Ter)	ACVRL1 (E159*)	Single nucleotide variant (nonsense)	Telangiectasia, hereditary hemorrhagic, type 2	GPathogenic
Select item 982485	NM_000020.3(ACVRL1):c.375dup (p.Val126fs)	ACVRL1 (V126fs)	Duplication (frameshift variant)	Telangiectasia, hereditary hemorrhagic, type 2	GPathogenic
Select item 982484	NM_001114753.3(ENG):c.899_901delinsC (p.Leu300fs)	ENG (L118fs +1 more)	Indel (frameshift variant)	Telangiectasia, hereditary hemorrhagic, type 1	GPathogenic
Select item 982483	NM_001114753.3(ENG):c.896T>G (p.Leu299Arg)	ENG (L117R +1 more)	Single nucleotide variant (missense variant)	Telangiectasia, hereditary hemorrhagic, type 1 +1 more	GLikely pathogenic
Select item 982482	NM_001114753.3(ENG):c.817-1G>A	ENG	Single nucleotide variant (splice acceptor variant)	Telangiectasia, hereditary hemorrhagic, type 1	GPathogenic
Select item 982481	NM_001114753.3(ENG):c.776T>G (p.Val259Gly)	ENG (V259G +1 more)	Single nucleotide variant (missense variant)	Telangiectasia, hereditary hemorrhagic, type 1	GUncertain significance
Select item 982480	NM_001114753.3(ENG):c.772del (p.Tyr258fs)	ENG (Y258fs +1 more)	Deletion (frameshift variant)	Telangiectasia, hereditary hemorrhagic, type 1 +3 more	GPathogenic
Select item 982479	NM_001114753.3(ENG):c.761_767dup (p.Pro257fs)	ENG (P257fs +1 more)	Duplication (frameshift variant)	Telangiectasia, hereditary hemorrhagic, type 1	GPathogenic
Select item 982478	NM_001114753.3(ENG):c.763G>T (p.Gly255Cys)	ENG (G255C +1 more)	Single nucleotide variant (missense variant)	Telangiectasia, hereditary hemorrhagic, type 1	GLikely pathogenic
Select item 982477	NM_001114753.3(ENG):c.690-2A>G	ENG	Single nucleotide variant (splice acceptor variant)	Telangiectasia, hereditary hemorrhagic, type 1	GPathogenic
Select item 982476	NM_001114753.3(ENG):c.667dup (p.Val223fs)	ENG (V223fs +1 more)	Duplication (frameshift variant)	Telangiectasia, hereditary hemorrhagic, type 1	GPathogenic
Select item 982475	NM_001114753.3(ENG):c.646A>G (p.Lys216Glu)	ENG (K216E +1 more)	Single nucleotide variant (missense variant)	Telangiectasia, hereditary hemorrhagic, type 1 +1 more	GConflicting classifications of pathogenicity
Select item 982474	NM_001114753.3(ENG):c.63dup (p.Thr22fs)	ENG (T22fs)	Duplication (frameshift variant)	Telangiectasia, hereditary hemorrhagic, type 1	GPathogenic
Select item 982473	NM_001114753.3(ENG):c.298_299del (p.Ser100fs)	ENG (S100fs)	Deletion (frameshift variant +1 more)	Telangiectasia, hereditary hemorrhagic, type 1	GPathogenic
Select item 982472	NM_001114753.3(ENG):c.239T>C (p.Leu80Pro)	ENG (L80P)	Single nucleotide variant (missense variant +1 more)	Telangiectasia, hereditary hemorrhagic, type 1	GUncertain significance
Select item 982471	NM_001114753.3(ENG):c.208G>T (p.Glu70Ter)	ENG (E70*)	Single nucleotide variant (nonsense +1 more)	Telangiectasia, hereditary hemorrhagic, type 1	GPathogenic
Select item 982470	NM_001114753.3(ENG):c.164del (p.Ala55fs)	ENG (A55fs)	Deletion (frameshift variant +1 more)	Telangiectasia, hereditary hemorrhagic, type 1 +1 more	GPathogenic
Select item 982469	NM_001114753.3(ENG):c.1626del (p.Thr544fs)	ENG, LOC102723566 (T362fs +1 more)	Deletion (frameshift variant)	Telangiectasia, hereditary hemorrhagic, type 1	GPathogenic
Select item 982468	NM_001114753.3(ENG):c.1582_1583del (p.Pro528fs)	ENG, LOC102723566 (P346fs +1 more)	Deletion (frameshift variant)	Telangiectasia, hereditary hemorrhagic, type 1	GPathogenic
Select item 982467	NM_001114753.3(ENG):c.1513G>T (p.Glu505Ter)	LOC102723566, ENG (E323* +1 more)	Single nucleotide variant (nonsense)	Cardiovascular phenotype +1 more	GPathogenic
Select item 982466	NM_001114753.3(ENG):c.1490dup (p.Leu497fs)	ENG, LOC102723566 (L315fs +1 more)	Duplication (frameshift variant +1 more)	Telangiectasia, hereditary hemorrhagic, type 1	GPathogenic
Select item 982465	Single allele	ENG	Deletion	Telangiectasia, hereditary hemorrhagic, type 1	GPathogenic
Select item 982464	NM_001114753.3(ENG):c.68-4227_219+104del	ENG	Deletion (splice acceptor variant +1 more)	Telangiectasia, hereditary hemorrhagic, type 1	GPathogenic
Select item 982463	NM_001114753.3(ENG):c.220-225_991+123del	ENG	Deletion (splice acceptor variant +2 more)	Telangiectasia, hereditary hemorrhagic, type 1	GPathogenic
Select item 982462	NM_001114753.3(ENG):c.523+229_991+123del	ENG	Deletion (splice acceptor variant +2 more)	Telangiectasia, hereditary hemorrhagic, type 1	GPathogenic
Select item 982461	NM_001114753.3(ENG):c.220-988_1134+331del	ENG	Deletion (splice acceptor variant +2 more)	Telangiectasia, hereditary hemorrhagic, type 1	GPathogenic
Select item 982460	NM_001114753.3(ENG):c.220-226_1134+331del	ENG	Deletion (splice acceptor variant +2 more)	Telangiectasia, hereditary hemorrhagic, type 1	GPathogenic
Select item 982459	Single allele	ENG	Deletion	Telangiectasia, hereditary hemorrhagic, type 1	GPathogenic
Select item 982458	NC_000009.12:g.127814980_127830815del	ENG, LOC102723566	Deletion	Telangiectasia, hereditary hemorrhagic, type 1	GPathogenic
Select item 982457	NC_000009.12:g.127814982_127820052del	ENG, LOC102723566	Deletion	Telangiectasia, hereditary hemorrhagic, type 1	GPathogenic
Select item 982456	NM_001114753.3(ENG):c.524-1_689+1del	ENG	Deletion (splice acceptor variant +2 more)	Telangiectasia, hereditary hemorrhagic, type 1	GPathogenic
Select item 982455	NM_005359.6(SMAD4):c.303G>A (p.Trp101Ter)	SMAD4 (W101*)	Single nucleotide variant (nonsense)	Hereditary cancer-predisposing syndrome +2 more	GPathogenic
Select item 982454	NM_000020.3(ACVRL1):c.259del (p.His87fs)	ACVRL1 (H87fs)	Deletion (frameshift variant)	Telangiectasia, hereditary hemorrhagic, type 2	GPathogenic
Select item 982453	NM_000020.3(ACVRL1):c.1459A>C (p.Lys487Gln)	ACVRL1 (K487Q)	Single nucleotide variant (missense variant)	Telangiectasia, hereditary hemorrhagic, type 2	GLikely pathogenic
Select item 982452	NM_000020.3(ACVRL1):c.1457AGA[1] (p.Lys487del)	ACVRL1 (K487del)	Microsatellite (inframe_deletion)	Telangiectasia, hereditary hemorrhagic, type 2 +2 more	GConflicting classifications of pathogenicity
Select item 982451	NM_000020.3(ACVRL1):c.1448del (p.Leu483fs)	ACVRL1 (L483fs)	Deletion (frameshift variant)	Telangiectasia, hereditary hemorrhagic, type 2	GPathogenic
Select item 982450	NM_000020.3(ACVRL1):c.139dup (p.Arg47fs)	ACVRL1 (R47fs)	Duplication (frameshift variant)	Telangiectasia, hereditary hemorrhagic, type 2 +1 more	GPathogenic
Select item 982449	NM_000020.3(ACVRL1):c.1298C>A (p.Pro433His)	ACVRL1 (P433H)	Single nucleotide variant (missense variant)	Telangiectasia, hereditary hemorrhagic, type 2	GLikely pathogenic
Select item 982448	NM_000020.3(ACVRL1):c.1246+5G>A	ACVRL1	Single nucleotide variant (intron variant)	Telangiectasia, hereditary hemorrhagic, type 2 +1 more	GConflicting classifications of pathogenicity
Select item 982447	NM_000020.3(ACVRL1):c.1171G>T (p.Glu391Ter)	ACVRL1 (E391*)	Single nucleotide variant (nonsense)	Telangiectasia, hereditary hemorrhagic, type 2	GPathogenic
Select item 982446	NM_000020.3(ACVRL1):c.1153A>C (p.Ile385Leu)	ACVRL1 (I385L)	Single nucleotide variant (missense variant)	Telangiectasia, hereditary hemorrhagic, type 2	GLikely benign
Select item 982445	NM_000020.3(ACVRL1):c.1041del (p.Asp348fs)	ACVRL1 (D348fs)	Deletion (frameshift variant)	Telangiectasia, hereditary hemorrhagic, type 2	GPathogenic
Select item 982444	NM_000020.3(ACVRL1):c.1037_1039del (p.Ile346_Ala347delinsThr)	ACVRL1	Deletion (inframe_indel)	Telangiectasia, hereditary hemorrhagic, type 2	GConflicting classifications of pathogenicity
Select item 982291	NM_015175.3(NBEAL2):c.7501C>T (p.His2501Tyr)	NBEAL2 (H2467Y +1 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 982290	NM_015175.3(NBEAL2):c.1476_1479dup (p.Leu494fs)	NBEAL2 (L460fs +1 more)	Microsatellite (frameshift variant)	Gray platelet syndrome	GPathogenic
Select item 982289	NM_015175.3(NBEAL2):c.6894T>A (p.Asn2298Lys)	NBEAL2 (N2264K +1 more)	Single nucleotide variant (missense variant)	Gray platelet syndrome	GLikely pathogenic
Select item 982288	NM_015175.3(NBEAL2):c.7134G>A (p.Glu2378=)	NBEAL2	Single nucleotide variant (synonymous variant)	Gray platelet syndrome	GUncertain significance
Select item 982287	NM_015175.3(NBEAL2):c.3058T>C (p.Tyr1020His)	NBEAL2 (Y1020H +1 more)	Single nucleotide variant (missense variant)	Gray platelet syndrome	GUncertain significance
Select item 982286	NM_015175.3(NBEAL2):c.2650-1G>A	NBEAL2	Single nucleotide variant (splice acceptor variant)	Gray platelet syndrome	GPathogenic
Select item 982285	NM_015175.3(NBEAL2):c.5935C>T (p.Arg1979Trp)	NBEAL2 (R1945W +1 more)	Single nucleotide variant (missense variant)	Gray platelet syndrome	GUncertain significance
Select item 982284	NM_015175.3(NBEAL2):c.2552C>T (p.Pro851Leu)	NBEAL2 (P817L +1 more)	Single nucleotide variant (missense variant)	Gray platelet syndrome	GUncertain significance
Select item 982283	NM_015175.3(NBEAL2):c.1933TTC[1] (p.Phe646del)	NBEAL2 (F612del +1 more)	Microsatellite (inframe_deletion)	Gray platelet syndrome	GUncertain significance
Select item 982282	NM_015175.3(NBEAL2):c.4485-1G>T	NBEAL2	Single nucleotide variant (splice acceptor variant)	Gray platelet syndrome	GPathogenic
Select item 982281	NM_015175.3(NBEAL2):c.7937T>C (p.Leu2646Pro)	NBEAL2 (L2612P +1 more)	Single nucleotide variant (missense variant)	Gray platelet syndrome	GUncertain significance
Select item 982280	NM_015175.3(NBEAL2):c.6568del (p.Cys2190fs)	NBEAL2 (C2156fs +1 more)	Deletion (frameshift variant)	Gray platelet syndrome	GPathogenic
Select item 982279	NM_015175.3(NBEAL2):c.6920-1G>C	NBEAL2	Single nucleotide variant (splice acceptor variant)	Gray platelet syndrome	GPathogenic
Select item 982278	NM_015175.3(NBEAL2):c.7506del (p.Asp2503fs)	NBEAL2 (D2469fs +1 more)	Deletion (frameshift variant)	Gray platelet syndrome	GPathogenic
Select item 982277	NM_015175.3(NBEAL2):c.4890del (p.Arg1631fs)	NBEAL2 (R1597fs +1 more)	Deletion (frameshift variant)	Gray platelet syndrome	GPathogenic
Select item 982276	NM_015175.3(NBEAL2):c.7192_7202dup (p.Gln2402fs)	NBEAL2 (Q2368fs +1 more)	Duplication (frameshift variant)	Gray platelet syndrome	GPathogenic
Select item 982275	NM_015175.3(NBEAL2):c.6202T>C (p.Trp2068Arg)	NBEAL2 (W2034R +1 more)	Single nucleotide variant (missense variant)	Gray platelet syndrome	GUncertain significance
Select item 982274	NM_015175.3(NBEAL2):c.4928_4929del (p.Asp1643fs)	NBEAL2 (D1609fs +1 more)	Deletion (frameshift variant)	Gray platelet syndrome	GPathogenic
Select item 982273	NM_015175.3(NBEAL2):c.3774_3780delinsCAGCGTTCGCCTCAGA (p.Asp1259_Ile1260delinsSerValArgLeuArg)	NBEAL2	Indel (inframe_indel)	Gray platelet syndrome	GUncertain significance
Select item 982272	NM_015175.3(NBEAL2):c.2751dup (p.Asp918Ter)	NBEAL2 (D884* +1 more)	Duplication (nonsense)	Gray platelet syndrome	GPathogenic
Select item 982271	NM_015175.3(NBEAL2):c.427G>A (p.Glu143Lys)	NBEAL2 (E136K +1 more)	Single nucleotide variant (missense variant)	Gray platelet syndrome	GUncertain significance
Select item 982270	NM_015175.3(NBEAL2):c.1725_1728dup (p.Ala577fs)	NBEAL2 (A543fs +1 more)	Duplication (frameshift variant)	Gray platelet syndrome	GPathogenic
Select item 974775	NM_001159699.2(FHL1):c.710G>A (p.Cys237Tyr)	FHL1 (C221Y +2 more)	Single nucleotide variant (missense variant +2 more)	Asymmetric septal hypertrophy	GLikely pathogenic
Select item 974774	NM_001458.5(FLNC):c.6004+2T>C	FLNC, FLNC-AS1	Single nucleotide variant (splice donor variant)	Hypertrophic cardiomyopathy 26 +1 more	GLikely pathogenic
Select item 949536	NM_001114753.3(ENG):c.774C>A (p.Tyr258Ter)	ENG (Y76* +1 more)	Single nucleotide variant (nonsense)	Telangiectasia, hereditary hemorrhagic, type 1 +1 more	GPathogenic
Select item 946806	NM_001114753.3(ENG):c.159C>A (p.Cys53Ter)	ENG (C53*)	Single nucleotide variant (nonsense +1 more)	Hereditary hemorrhagic telangiectasia +2 more	GPathogenic
Select item 944925	NM_001114753.3(ENG):c.777_778dup (p.Ser260fs)	ENG (S260fs +1 more)	Microsatellite (frameshift variant)	Telangiectasia, hereditary hemorrhagic, type 1 +1 more	GPathogenic
Select item 941644	NM_000020.3(ACVRL1):c.830C>A (p.Thr277Lys)	ACVRL1 (T277K)	Single nucleotide variant (missense variant)	ACVRL1-related disorder +3 more	GPathogenic/Likely pathogenic
Select item 872911	NM_000132.4(F8):c.5993A>T (p.Tyr1998Phe)	F8 (Y1998F)	Single nucleotide variant (missense variant)	Hereditary factor VIII deficiency disease	GLikely benign
Select item 842548	NM_001114753.3(ENG):c.1472_1475del (p.Asp491fs)	ENG, LOC102723566 (D309fs +1 more)	Deletion (frameshift variant +1 more)	Hereditary hemorrhagic telangiectasia +2 more	GPathogenic/Likely pathogenic

<< First< Prev

Page of 10