All transcript variants in gene HNRNPAB

Information The variants shown are described using the NM_004499.3 transcript reference sequence.

67 entries on 1 page. Showing entries 1 - 67.
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Effect     

AscendingDNA change (cDNA)     

RNA change     

Protein     

DNA change (genomic) (hg19)     

Reference     

DB-ID     

Frequency     

Freq. EA     

Freq. AA     
?/? c.12G>A r.(=) p.(=) g.177631850G>A Copied from the Exome Variant Server HNRNPAB_000001 4/6418 0/4216 4/2202
?/? c.209+23del r.(=) p.(=) g.177632070del Copied from the Exome Variant Server HNRNPAB_000002 40/5854 1/3748 39/2106
?/? c.210-42C>T r.(=) p.(=) g.177632801C>T Copied from the Exome Variant Server HNRNPAB_000003 264/13006 236/8600 28/4406
?/? c.210-26C>T r.(=) p.(=) g.177632817C>T Copied from the Exome Variant Server HNRNPAB_000004 1/13006 1/8600 0/4406
?/? c.233G>C r.(?) p.(Ser78Thr) g.177632866G>C Copied from the Exome Variant Server HNRNPAB_000005 1/13006 0/8600 1/4406
?/? c.243T>A r.(=) p.(=) g.177632876T>A Copied from the Exome Variant Server HNRNPAB_000006 2/13006 2/8600 0/4406
?/? c.258_259del r.(?) p.(Lys87Argfs*5) g.177632891_177632892del Copied from the Exome Variant Server HNRNPAB_000007 24/12518 14/8254 10/4264
?/? c.285G>A r.(=) p.(=) g.177632918G>A Copied from the Exome Variant Server HNRNPAB_000008 1/13006 1/8600 0/4406
?/? c.320C>G r.(?) p.(Thr107Ser) g.177632953C>G Copied from the Exome Variant Server HNRNPAB_000009 2/13006 2/8600 0/4406
?/? c.357A>G r.(=) p.(=) g.177632990A>G Copied from the Exome Variant Server HNRNPAB_000010 1/13006 1/8600 0/4406
?/? c.378+4A>T r.spl? p.? g.177633015A>T Copied from the Exome Variant Server HNRNPAB_000011 1/13006 1/8600 0/4406
?/? c.378+17A>G r.(=) p.(=) g.177633028A>G Copied from the Exome Variant Server HNRNPAB_000012 1/13006 1/8600 0/4406
?/? c.378+22A>G r.(=) p.(=) g.177633033A>G Copied from the Exome Variant Server HNRNPAB_000013 1/13006 1/8600 0/4406
?/? c.379-52C>T r.(=) p.(=) g.177633681C>T Copied from the Exome Variant Server HNRNPAB_000014 1/5734 1/3982 0/1752
?/? c.379-39G>A r.(=) p.(=) g.177633694G>A Copied from the Exome Variant Server HNRNPAB_000015 1/13006 1/8600 0/4406
?/? c.379-30A>T r.(=) p.(=) g.177633703A>T Copied from the Exome Variant Server HNRNPAB_000016 34/13006 32/8600 2/4406
?/? c.379-24C>A r.(=) p.(=) g.177633709C>A Copied from the Exome Variant Server HNRNPAB_000017 1/13006 1/8600 0/4406
?/? c.456G>A r.(=) p.(=) g.177633810G>A Copied from the Exome Variant Server HNRNPAB_000018 1/13006 1/8600 0/4406
?/? c.471C>T r.(=) p.(=) g.177633825C>T Copied from the Exome Variant Server HNRNPAB_000019 1/13006 1/8600 0/4406
?/? c.518A>T r.(?) p.(Tyr173Phe) g.177633872A>T Copied from the Exome Variant Server HNRNPAB_000020 3/13006 3/8600 0/4406
?/? c.537+25C>T r.(=) p.(=) g.177633916C>T Copied from the Exome Variant Server HNRNPAB_000021 1/13006 0/8600 1/4406
?/? c.537+35C>T r.(=) p.(=) g.177633926C>T Copied from the Exome Variant Server HNRNPAB_000022 1/13006 1/8600 0/4406
?/? c.538-42G>A r.(=) p.(=) g.177634053G>A Copied from the Exome Variant Server HNRNPAB_000023 1/13006 1/8600 0/4406
?/? c.548T>C r.(?) p.(Ile183Thr) g.177634105T>C Copied from the Exome Variant Server HNRNPAB_000024 2/13006 2/8600 0/4406
?/? c.559A>T r.(?) p.(Met187Leu) g.177634116A>T Copied from the Exome Variant Server HNRNPAB_000025 3/13006 3/8600 0/4406
?/? c.624_626del r.(?) p.(Lys210del) g.177634181_177634183del Copied from the Exome Variant Server HNRNPAB_000026 1/12514 1/8250 0/4264
?/? c.657C>T r.(=) p.(=) g.177634214C>T Copied from the Exome Variant Server HNRNPAB_000027 1/13006 1/8600 0/4406
?/? c.669+5G>A r.spl? p.? g.177634231G>A Copied from the Exome Variant Server HNRNPAB_000028 12/13006 12/8600 0/4406
?/? c.669+31T>C r.(=) p.(=) g.177634257T>C Copied from the Exome Variant Server HNRNPAB_000029 1/13002 0/8600 1/4402
?/? c.670-37G>A r.(=) p.(=) g.177636294G>A Copied from the Exome Variant Server HNRNPAB_000030 1/13006 1/8600 0/4406
?/? c.728G>C r.(?) p.(Gly243Ala) g.177636389G>C Copied from the Exome Variant Server HNRNPAB_000031 1/13006 0/8600 1/4406
?/? c.734G>A r.(?) p.(Arg245His) g.177636395G>A Copied from the Exome Variant Server HNRNPAB_000032 2/13006 0/8600 2/4406
?/? c.742C>T r.(?) p.(Arg248Cys) g.177636403C>T Copied from the Exome Variant Server HNRNPAB_000033 1/13006 1/8600 0/4406
?/? c.761G>A r.(?) p.(Gly254Asp) g.177636422G>A Copied from the Exome Variant Server HNRNPAB_000034 10/13006 9/8600 1/4406
?/? c.764G>A r.(?) p.(Ser255Asn) g.177636425G>A Copied from the Exome Variant Server HNRNPAB_000035 1/13006 1/8600 0/4406
?/? c.787+28C>A r.(=) p.(=) g.177636476C>A Copied from the Exome Variant Server HNRNPAB_000036 243/13006 2/8600 241/4406
?/? c.787+40C>T r.(=) p.(=) g.177636488C>T Copied from the Exome Variant Server HNRNPAB_000037 34/13006 0/8600 34/4406
?/? c.787+50G>C r.(=) p.(=) g.177636498G>C Copied from the Exome Variant Server HNRNPAB_000038 1/13004 1/8598 0/4406
?/? c.787+51C>T r.(=) p.(=) g.177636499C>T Copied from the Exome Variant Server HNRNPAB_000039 1/13004 1/8598 0/4406
?/? c.788-457T>C r.(=) p.(=) g.177637097T>C Copied from the Exome Variant Server HNRNPAB_000041 1/13006 1/8600 0/4406
?/? c.788-427C>T r.(=) p.(=) g.177637127C>T Copied from the Exome Variant Server HNRNPAB_000043 1/13006 1/8600 0/4406
?/? c.788-426C>G r.(=) p.(=) g.177637128C>G Copied from the Exome Variant Server HNRNPAB_000045 1/13006 1/8600 0/4406
?/? c.788-416A>T r.(=) p.(=) g.177637138A>T Copied from the Exome Variant Server HNRNPAB_000047 1/13006 1/8600 0/4406
?/? c.788-405G>C r.(=) p.(=) g.177637149G>C Copied from the Exome Variant Server HNRNPAB_000049 1/13006 1/8600 0/4406
?/? c.788-404A>G r.(=) p.(=) g.177637150A>G Copied from the Exome Variant Server HNRNPAB_000051 1/13006 1/8600 0/4406
?/? c.788-369C>T r.(=) p.(=) g.177637185C>T Copied from the Exome Variant Server HNRNPAB_000053 1/13006 1/8600 0/4406
?/? c.788-350G>A r.(=) p.(=) g.177637204G>A Copied from the Exome Variant Server HNRNPAB_000055 1/13006 1/8600 0/4406
?/? c.788-335G>A r.(=) p.(=) g.177637219G>A Copied from the Exome Variant Server HNRNPAB_000040 10/13006 0/8600 10/4406
?/? c.788-310A>G r.(=) p.(=) g.177637244A>G Copied from the Exome Variant Server HNRNPAB_000042 3/13006 0/8600 3/4406
?/? c.788-293G>A r.(=) p.(=) g.177637261G>A Copied from the Exome Variant Server HNRNPAB_000044 1/13006 1/8600 0/4406
?/? c.788-253C>T r.(=) p.(=) g.177637301C>T Copied from the Exome Variant Server HNRNPAB_000046 1/13004 1/8598 0/4406
?/? c.788-244C>T r.(=) p.(=) g.177637310C>T Copied from the Exome Variant Server HNRNPAB_000048 7/13002 1/8596 6/4406
?/? c.788-64T>C r.(=) p.(=) g.177637490T>C Copied from the Exome Variant Server HNRNPAB_000050 1/4566 1/3182 0/1384
?/? c.788-63C>G r.(=) p.(=) g.177637491C>G Copied from the Exome Variant Server HNRNPAB_000052 2/4566 0/3182 2/1384
?/? c.788-45C>T r.(=) p.(=) g.177637509C>T Copied from the Exome Variant Server HNRNPAB_000054 1/13006 1/8600 0/4406
?/? c.788-28T>G r.(=) p.(=) g.177637526T>G Copied from the Exome Variant Server HNRNPAB_000056 1/13006 1/8600 0/4406
?/? c.788-13T>C r.(=) p.(=) g.177637541T>C Copied from the Exome Variant Server HNRNPAB_000057 24/13006 0/8600 24/4406
?/? c.788-9C>T r.(=) p.(=) g.177637545C>T Copied from the Exome Variant Server HNRNPAB_000058 1/13006 1/8600 0/4406
?/? c.788-8G>A r.(=) p.(=) g.177637546G>A Copied from the Exome Variant Server HNRNPAB_000059 1/13006 1/8600 0/4406
?/? c.795T>C r.(=) p.(=) g.177637561T>C Copied from the Exome Variant Server HNRNPAB_000060 181/13006 0/8600 181/4406
?/? c.800C>T r.(?) p.(Thr267Ile) g.177637566C>T Copied from the Exome Variant Server HNRNPAB_000061 1/13006 1/8600 0/4406
?/? c.*3C>T r.(=) p.(=) g.177637627C>T Copied from the Exome Variant Server HNRNPAB_000062 1/13006 0/8600 1/4406
?/? c.*10A>G r.(=) p.(=) g.177637634A>G Copied from the Exome Variant Server HNRNPAB_000063 22/13006 20/8600 2/4406
?/? c.*11G>A r.(=) p.(=) g.177637635G>A Copied from the Exome Variant Server HNRNPAB_000064 1/13006 1/8600 0/4406
?/? c.*28G>A r.(=) p.(=) g.177637652G>A Copied from the Exome Variant Server HNRNPAB_000065 7/13006 7/8600 0/4406
?/? c.*36G>T r.(=) p.(=) g.177637660G>T Copied from the Exome Variant Server HNRNPAB_000066 3/13006 0/8600 3/4406
?/? c.*50T>C r.(=) p.(=) g.177637674T>C Copied from the Exome Variant Server HNRNPAB_000067 25/13006 0/8600 25/4406
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