All transcript variants in gene H2BFWT

Information The variants shown are described using the NM_001002916.3 transcript reference sequence.

40 entries on 1 page. Showing entries 1 - 40.
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Effect     

AscendingDNA change (cDNA)     

RNA change     

Protein     

DNA change (genomic) (hg19)     

Reference     

DB-ID     

Frequency     

Freq. EA     

Freq. AA     
?/? c.-24G>A r.(=) p.(=) g.103268256C>T Copied from the Exome Variant Server H2BFWT_000040 1/10548 1/6717 0/3831
?/? c.-14C>T r.(=) p.(=) g.103268246G>A Copied from the Exome Variant Server H2BFWT_000039 3/10559 1/6728 2/3831
?/? c.-9C>T r.(=) p.(=) g.103268241G>A Copied from the Exome Variant Server H2BFWT_000038 3195/10556 2894/6726 301/3830
?/? c.8G>A r.(?) p.(Arg3His) g.103268225C>T Copied from the Exome Variant Server H2BFWT_000037 1/10559 1/6726 0/3833
?/? c.13G>A r.(?) p.(Glu5Lys) g.103268220C>T Copied from the Exome Variant Server H2BFWT_000036 1/10561 0/6727 1/3834
?/? c.23G>A r.(?) p.(Arg8Gln) g.103268210C>T Copied from the Exome Variant Server H2BFWT_000035 1/10560 0/6726 1/3834
?/? c.32G>A r.(?) p.(Arg11Gln) g.103268201C>T Copied from the Exome Variant Server H2BFWT_000034 1/10562 1/6727 0/3835
?/? c.43G>A r.(?) p.(Ala15Thr) g.103268190C>T Copied from the Exome Variant Server H2BFWT_000033 1/10562 0/6727 1/3835
?/? c.56C>T r.(?) p.(Ser19Leu) g.103268177G>A Copied from the Exome Variant Server H2BFWT_000032 18/10563 0/6728 18/3835
?/? c.57G>A r.(=) p.(=) g.103268176C>T Copied from the Exome Variant Server H2BFWT_000031 1/10563 0/6728 1/3835
?/? c.60C>A r.(?) p.(Cys20*) g.103268173G>T Copied from the Exome Variant Server H2BFWT_000030 1/10563 0/6728 1/3835
?/? c.81C>T r.(=) p.(=) g.103268152G>A Copied from the Exome Variant Server H2BFWT_000029 1/10563 1/6728 0/3835
?/? c.82G>A r.(?) p.(Ala28Thr) g.103268151C>T Copied from the Exome Variant Server H2BFWT_000028 10/10563 0/6728 10/3835
?/? c.108G>C r.(=) p.(=) g.103268125C>G Copied from the Exome Variant Server H2BFWT_000027 3/10563 3/6728 0/3835
?/? c.195G>A r.(=) p.(=) g.103268038C>T Copied from the Exome Variant Server H2BFWT_000026 1/10563 1/6728 0/3835
?/? c.205C>T r.(?) p.(Pro69Ser) g.103268028G>A Copied from the Exome Variant Server H2BFWT_000025 3/10563 3/6728 0/3835
?/? c.230G>A r.(?) p.(Arg77His) g.103268003C>T Copied from the Exome Variant Server H2BFWT_000024 1/10563 1/6728 0/3835
?/? c.232G>A r.(?) p.(Gly78Arg) g.103268001C>T Copied from the Exome Variant Server H2BFWT_000023 2/10563 0/6728 2/3835
?/? c.259C>T r.(?) p.(Arg87Trp) g.103267974G>A Copied from the Exome Variant Server H2BFWT_000022 199/10563 184/6728 15/3835
?/? c.285C>G r.(=) p.(=) g.103267948G>C Copied from the Exome Variant Server H2BFWT_000021 4/10563 0/6728 4/3835
?/? c.298C>T r.(?) p.(Arg100Trp) g.103267935G>A Copied from the Exome Variant Server H2BFWT_000020 1/10563 0/6728 1/3835
?/? c.347G>A r.(?) p.(Arg116His) g.103267886C>T Copied from the Exome Variant Server H2BFWT_000019 2/10563 0/6728 2/3835
?/? c.358G>A r.(?) p.(Glu120Lys) g.103267875C>T Copied from the Exome Variant Server H2BFWT_000018 1/10563 0/6728 1/3835
?/? c.368G>A r.(?) p.(Arg123His) g.103267865C>T Copied from the Exome Variant Server H2BFWT_000017 6734/10562 4476/6727 2258/3835
?/? c.376C>T r.(?) p.(Arg126Cys) g.103267857G>A Copied from the Exome Variant Server H2BFWT_000016 7/10563 7/6728 0/3835
?/? c.377G>T r.(?) p.(Arg126Leu) g.103267856C>A Copied from the Exome Variant Server H2BFWT_000015 4/10563 0/6728 4/3835
?/? c.408G>A r.(?) p.(Trp136*) g.103267825C>T Copied from the Exome Variant Server H2BFWT_000014 1/10563 1/6728 0/3835
?/? c.409G>A r.(?) p.(Glu137Lys) g.103267824C>T Copied from the Exome Variant Server H2BFWT_000013 2/10563 2/6728 0/3835
?/? c.413C>T r.(?) p.(Thr138Ile) g.103267820G>A Copied from the Exome Variant Server H2BFWT_000012 10/10563 9/6728 1/3835
?/? c.462C>T r.(=) p.(=) g.103267771G>A Copied from the Exome Variant Server H2BFWT_000011 1/10552 1/6721 0/3831
?/? c.468C>G r.(=) p.(=) g.103267765G>C Copied from the Exome Variant Server H2BFWT_000010 1/10553 1/6723 0/3830
?/? c.476C>T r.(?) p.(Thr159Met) g.103267757G>A Copied from the Exome Variant Server H2BFWT_000009 1/10551 0/6721 1/3830
?/? c.491+19C>T r.(=) p.(=) g.103267723G>A Copied from the Exome Variant Server H2BFWT_000008 2/10540 2/6711 0/3829
?/? c.492-30C>G r.(=) p.(=) g.103267350G>C Copied from the Exome Variant Server H2BFWT_000007 1/10563 1/6728 0/3835
?/? c.492-22A>T r.(=) p.(=) g.103267342T>A Copied from the Exome Variant Server H2BFWT_000006 1/10563 0/6728 1/3835
?/? c.492-7T>C r.(=) p.(=) g.103267327A>G Copied from the Exome Variant Server H2BFWT_000005 3/10563 1/6728 2/3835
?/? c.510del r.(?) p.(Gln171Serfs*20) g.103267302del Copied from the Exome Variant Server H2BFWT_000004 7/10205 7/6484 0/3721
?/? c.521_522del r.(?) p.(Arg174Lysfs*20) g.103267290_103267291del Copied from the Exome Variant Server H2BFWT_000003 3/10205 0/6484 3/3721
?/? c.522A>G r.(=) p.(=) g.103267290T>C Copied from the Exome Variant Server H2BFWT_000002 5/10563 3/6728 2/3835
?/? c.523A>C r.(?) p.(Lys175Gln) g.103267289T>G Copied from the Exome Variant Server H2BFWT_000001 2/10563 2/6728 0/3835
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