Transcript #00000017 (NM_000038.5, APC gene)

Transcript name adenomatous polyposis coli, transcript variant 3
Gene name APC (APC, WNT signaling pathway regulator)
Chromosome 5
Transcript - NCBI ID NM_000038.5
Transcript - Ensembl ID -
Protein - NCBI ID NP_000029.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

35 entries on 1 page. Showing entries 1 - 35.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

Published as     

RNA change     

Protein     

GVS function     

Clinical classification     
+/. 11 c.847C>T R283X r.(?) p.(Arg283*) - ClinVar
+/. 9 c.847C>T R283∗ r.(?) p.(Arg283*) - ClinVar
+/. - c.1500T>G Y482X, Y500X r.(?) p.(Tyr500*) - Pathogenic
-/. - c.1984_1985del 1984-1985delCT r.(?) p.(Leu662Thrfs*11) - -
+/. 16 c.2334_2337del N778fs r.(?) p.(Asn778Lysfs*41) - ClinVar
+/. - c.2413C>T - r.(?) p.(Arg805*) - Pathogenic
+/. 16 c.2413C>T R805* r.(?) p.(Arg805*) - ClinVar
+/. 16 c.2802_2805del Y935fs r.(?) p.(Tyr935Ilefs*19) - ClinVar
+/. - c.2804dupA - r.(?) p.(Tyr935*) - Pathogenic/Likely pathogenic
+?/. 16 c.3139G>T E1057* r.(?) p.(Glu1047*) - ClinVar
?/. - c.3889_3890del c.3889-3890delGA r.(?) p.(Asp1297Phefs*3) - -
+/. 18 c.3927_3931del 3927-3931delAAAGA , codon 1309 r.(?) p.(Glu1309Aspfs*4) - ClinVar
?/. - c.3928_3929del 3928-3929delAA r.(?) p.(Lys1310Aspfs*4) - -
?/. 18 c.3928_3929del c.3928-3929delAA r.(?) p.(Lys1310Aspfs*4) - -
+/. - c.4031C>G S1326X, S1344X r.(?) p.(Ser1344*) - -
+/. - c.4033G>T E1304X, E1322X r.(?) p.(Glu1345*) - Pathogenic
+/. 16 c.4132C>T Q1378* r.(?) p.(Gln1378*) - ClinVar
+?/. 16 c.4135G>T E1361* r.(?) p.(Glu1379*) - ClinVar
?/. - c.4180_4183delGATA 4180-4183delGATA , codon 1394 r.(?) p.(Asp1394Valfs*20) - -
?/. - c.4182_4185delTAGT - r.(?) p.(Ser1395Leufs*19) - -
?/. - c.4197_4207del 4197-4207delTTCGATTGCCA r.(?) p.(Ser1400Leufs*5) - -
?/. 18 c.4199C>A S1400X r.(?) p.(Ser1400*) - -
+/. - c.4202_4203delTT - r.(?) p.(Ile1401Serfs*7) - -
?/. - c.4220_4221insAG - r.(?) p.(Ser1407Argfs*9) - -
+?/. - c.4285C>T Q1429X r.(?) p.(Gln1429*) - ClinVar
?/. 18 c.4348C>T 1450X r.(?) p.(Arg1450*) - ClinVar
+/. - c.4348C>T R1432X, R1450X r.(?) p.(Arg1450*) - Pathogenic
+/. - c.4348C>T 5214_5215GC, 5268_5269GC r.(?) p.(Arg1450*) - Pathogenic
?/. 18 c.4384_4385del 4384-4385delGA r.(?) p.(Lys1462Glufs*6) - ClinVar
+/. 16 c.4453del A1485fs r.(?) p.(Ala1485Leufs*22) - -
+/. - c.4455delT - r.(?) p.(Asp1486Ilefs*21) - -
-/. - c.4479G>A 112175770G > A r.(=) p.(=) - ClinVar
-/. - c.4479G>A 112175770G > A r.(=) p.(=) - ClinVar
?/. 11i_15i c.5959A>G - r.(?) p.(Ile1987Val) - ClinVar
?/. 11i_15i c.5995C>G - r.(?) p.(Pro1999Ala) - ClinVar
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