Transcript #00000049 (NM_000384.2, APOB gene)

Transcript name apolipoprotein B
Gene name APOB (apolipoprotein B)
Chromosome 2
Transcript - NCBI ID NM_000384.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_000375.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

44 entries on 1 page. Showing entries 1 - 44.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

Published as     

RNA change     

Protein     

GVS function     

Clinical classification     
+/. 1i c.82+77G>C - r.(=) p.(=) - -
+/. 3i c.237+296A>T - r.(=) p.(=) - -
+?/. 4i c.383+1054C>T - r.(=) p.(=) - -
+?/. 4i c.384-1015T>G - r.(=) p.(=) - -
+/. 5i c.538-77C>T - r.(=) p.(=) - -
./. 5i c.538-9C>T - r.(=) p.(=) - ClinVar
+?/. 7i c.819-154A>G - r.(=) p.(=) - -
+/. 12 c.1594C>T - r.(?) p.(Arg532Trp) - -
+?/. 14i c.2068-98T>C - r.(=) p.(=) - -
+/. 14i c.2068-4T>A - r.spl? p.? - -
+/. 16i c.2437-501A>T - r.(=) p.(=) - -
+?/. 17i c.2605-223T>A - r.(=) p.(=) - -
+?/. 18i c.2817-1223C>A - r.(=) p.(=) - -
+/. 18i c.2817-529G>A - r.(=) p.(=) - -
+?/. 19 c.2981C>T - r.(?) p.(Pro994Leu) - -
+?/. 20i c.3121+120G>A - r.(=) p.(=) - -
+?/. 20i c.3122-1017C>T - r.(=) p.(=) - -
+?/. 22 c.3337G>C - r.(?) p.(Asp1113His) - -
./. 25 c.4163G>A - r.(?) p.(Arg1388His) - ClinVar
+?/. 25i c.4217-42G>A - r.(=) p.(=) - -
+/. 26 c.7454A>G - r.(?) p.(Gln2485Arg) - -
-/. 26 c.7545C>T - r.(=) p.(=) - ClinVar
+/. 26 c.7545C>T - r.(=) p.(=) - Likely-Benign
./. 26 c.7619G>T - r.(?) p.(Gly2540Val) - ClinVar
+?/. 26 c.8039T>A - r.(?) p.(Leu2680Gln) - -
./. 26 c.8148C>T - r.(=) p.(=) - ClinVar
./. 26 c.8148C>T - r.(=) p.(=) - ClinVar
+/. 26 c.8216C>T - r.(?) p.(Pro2739Leu) - -
?/. 26 c.9544C>A - r.(?) p.(His3182Asn) - ClinVar
+/. 26 c.10576A>G - r.(?) p.(Thr3526Ala) - -
+/. 26 c.10700C>T - r.(?) p.(Thr3567Met) - Uncertain significance
+/. 26 c.10701G>A - r.(=) p.(=) - Likely-Benign
-?/. 26 c.10701G>T - r.(=) p.(=) - ClinVar
+/. 26 c.10996G>A - r.(?) p.(Glu3666Lys) - -
./. 27i c.11904-7C>T - r.(=) p.(=) - ClinVar
+?/. 29 c.12382G>A - r.(?) p.(Val4128Met) - -
+?/. 29 c.12541G>A - r.(?) p.(Glu4181Lys) - -
+?/. 29 c.12809G>C - r.(?) p.(Arg4270Thr) - -
+/. 29 c.12809G>C - r.(?) p.(Arg4270Thr) - -
+/. 29 c.12890G>A - r.(?) p.(Arg4297His) - Uncertain significance
?/. 29 c.12890G>A - r.(?) p.(Arg4297His) - ClinVar
+?/. 29 c.13013G>A - r.(?) p.(Ser4338Asn) - -
+/. 29 c.13013G>A - r.(?) p.(Ser4338Asn) - Benign
+/. 29 c.13028A>G - r.(?) p.(Tyr4343Cys) - Uncertain significance
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