All transcript variants in gene WAS

Information The variants shown are described using the NM_000377.2 transcript reference sequence.

61 entries on 1 page. Showing entries 1 - 61.
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Effect     

AscendingDNA change (cDNA)     

RNA change     

Protein     

DNA change (genomic) (hg19)     

Reference     

DB-ID     

Frequency     

Freq. EA     

Freq. AA     
?/? c.-23A>G r.(=) p.(=) g.48542220A>G Copied from the Exome Variant Server WAS_000004 2/10563 2/6728 0/3835
?/? c.30C>A r.(=) p.(=) g.48542272C>A Copied from the Exome Variant Server WAS_000005 2/10563 0/6728 2/3835
?/? c.56A>C r.(?) p.(Gln19Pro) g.48542298A>C Copied from the Exome Variant Server WAS_000008 1/10563 1/6728 0/3835
?/? c.74C>T r.(?) p.(Thr25Ile) g.48542316C>T Copied from the Exome Variant Server WAS_000010 1/10563 0/6728 1/3835
?/? c.90C>T r.(=) p.(=) g.48542332C>T Copied from the Exome Variant Server WAS_000012 12/10563 12/6728 0/3835
?/? c.101G>A r.(?) p.(Arg34Gln) g.48542343G>A Copied from the Exome Variant Server WAS_000001 1/10563 1/6728 0/3835
?/? c.132+30G>A r.(=) p.(=) g.48542404G>A Copied from the Exome Variant Server WAS_000002 14/10563 0/6728 14/3835
?/? c.184G>C r.(?) p.(Glu62Gln) g.48542723G>C Copied from the Exome Variant Server WAS_000003 1/10563 1/6728 0/3835
?/? c.206G>C r.(?) p.(Cys69Ser) g.48542745G>C Copied from the Exome Variant Server WAS_000006 2/10563 0/6728 2/3835
?/? c.249C>T r.(=) p.(=) g.48542788C>T Copied from the Exome Variant Server WAS_000007 1/10563 1/6728 0/3835
?/? c.264C>T r.(=) p.(=) g.48542803C>T Copied from the Exome Variant Server WAS_000009 1/10561 1/6727 0/3834
?/? c.266G>A r.(?) p.(Gly89Asp) g.48542805G>A Copied from the Exome Variant Server WAS_000011 3/10561 0/6727 3/3834
?/? c.273+4_273+5insC r.spl? p.? g.48542816_48542817insC Copied from the Exome Variant Server WAS_000013 260/10199 119/6479 141/3720
?/? c.274-46C>T r.(=) p.(=) g.48543890C>T Copied from the Exome Variant Server WAS_000014 1/10408 1/6614 0/3794
?/? c.274-45G>A r.(=) p.(=) g.48543891G>A Copied from the Exome Variant Server WAS_000015 1/10427 1/6627 0/3800
?/? c.274-42G>A r.(=) p.(=) g.48543894G>A Copied from the Exome Variant Server WAS_000016 1/10451 1/6649 0/3802
?/? c.351C>T r.(=) p.(=) g.48544013C>T Copied from the Exome Variant Server WAS_000017 2/10551 1/6718 1/3833
?/? c.360+36G>T r.(=) p.(=) g.48544058G>T Copied from the Exome Variant Server WAS_000018 1/10499 1/6680 0/3819
?/? c.391G>A r.(?) p.(Glu131Lys) g.48544153G>A Copied from the Exome Variant Server WAS_000019 24/10529 23/6702 1/3827
?/? c.413G>A r.(?) p.(Arg138Gln) g.48544175G>A Copied from the Exome Variant Server WAS_000021 9/10543 9/6713 0/3830
?/? c.463+50G>A r.(=) p.(=) g.48544275G>A Copied from the Exome Variant Server WAS_000023 1/10563 1/6728 0/3835
?/? c.470G>A r.(?) p.(Arg157His) g.48544341G>A Copied from the Exome Variant Server WAS_000025 1/10563 0/6728 1/3835
?/? c.505+20T>C r.(=) p.(=) g.48544396T>C Copied from the Exome Variant Server WAS_000027 1/10563 1/6728 0/3835
?/? c.505+30A>G r.(=) p.(=) g.48544406A>G Copied from the Exome Variant Server WAS_000029 1/10563 1/6728 0/3835
?/? c.524C>T r.(?) p.(Pro175Leu) g.48544488C>T Copied from the Exome Variant Server WAS_000031 1/10563 1/6728 0/3835
?/? c.538C>A r.(?) p.(His180Asn) g.48544502C>A Copied from the Exome Variant Server WAS_000033 14/10563 14/6728 0/3835
?/? c.559+4C>T r.spl? p.? g.48544527C>T Copied from the Exome Variant Server WAS_000035 1/10563 1/6728 0/3835
?/? c.559+73G>C r.(=) p.(=) g.48544596G>C Copied from the Exome Variant Server WAS_000037 9/3600 0/2391 9/1209
?/? c.560-50G>A r.(=) p.(=) g.48545120G>A Copied from the Exome Variant Server WAS_000039 1/10563 0/6728 1/3835
?/? c.560-46G>T r.(=) p.(=) g.48545124G>T Copied from the Exome Variant Server WAS_000041 1/10563 1/6728 0/3835
?/? c.593C>T r.(?) p.(Ala198Val) g.48545203C>T Copied from the Exome Variant Server WAS_000020 1/10563 0/6728 1/3835
?/? c.594G>A r.(=) p.(=) g.48545204G>A Copied from the Exome Variant Server WAS_000022 1/10563 1/6728 0/3835
?/? c.618C>T r.(=) p.(=) g.48545228C>T Copied from the Exome Variant Server WAS_000024 1/10563 1/6728 0/3835
?/? c.680G>A r.(?) p.(Arg227His) g.48545290G>A Copied from the Exome Variant Server WAS_000026 1/10563 1/6728 0/3835
?/? c.687_689del r.(?) p.(Lys232del) g.48545297_48545299del Copied from the Exome Variant Server WAS_000028 1/10205 0/6484 1/3721
?/? c.696G>A r.(=) p.(=) g.48545306G>A Copied from the Exome Variant Server WAS_000030 1/10563 1/6728 0/3835
?/? c.734+11C>T r.(=) p.(=) g.48545355C>T Copied from the Exome Variant Server WAS_000032 1/10561 0/6727 1/3834
?/? c.734+52A>G r.(=) p.(=) g.48545396A>G Copied from the Exome Variant Server WAS_000034 3/6033 0/3616 3/2417
?/? c.735-5C>T r.spl? p.? g.48546438C>T Copied from the Exome Variant Server WAS_000036 1/10563 0/6728 1/3835
?/? c.777+12_777+13insA r.(=) p.(=) g.48546497_48546498insA Copied from the Exome Variant Server WAS_000038 1/10203 0/6483 1/3720
?/? c.777+52C>T r.(=) p.(=) g.48546537C>T Copied from the Exome Variant Server WAS_000040 1/6038 1/3621 0/2417
?/? c.803G>A r.(?) p.(Arg268Gln) g.48546714G>A Copied from the Exome Variant Server WAS_000042 1/10563 0/6728 1/3835
?/? c.873C>T r.(=) p.(=) g.48546784C>T Copied from the Exome Variant Server WAS_000043 1/10563 1/6728 0/3835
?/? c.932-27C>A r.(=) p.(=) g.48547022C>A Copied from the Exome Variant Server WAS_000044 1/10522 1/6711 0/3811
?/? c.946C>A r.(?) p.(Pro316Thr) g.48547063C>A Copied from the Exome Variant Server WAS_000045 1/10477 1/6676 0/3801
?/? c.995T>C r.(?) p.(Val332Ala) g.48547112T>C Copied from the Exome Variant Server WAS_000046 32/10398 31/6633 1/3765
?/? c.999G>A r.(=) p.(=) g.48547116G>A Copied from the Exome Variant Server WAS_000047 1/10423 1/6645 0/3778
?/? c.1181C>T r.(?) p.(Pro394Leu) g.48547298C>T Copied from the Exome Variant Server WAS_000048 3/9726 0/6173 3/3553
?/? c.1200G>A r.(=) p.(=) g.48547317G>A Copied from the Exome Variant Server WAS_000049 2/9460 2/6016 0/3444
?/? c.1276G>T r.(?) p.(Ala426Ser) g.48547393G>T Copied from the Exome Variant Server WAS_000050 9/9934 0/6344 9/3590
?/? c.1299G>A r.(=) p.(=) g.48547416G>A Copied from the Exome Variant Server WAS_000051 1/10010 1/6394 0/3616
?/? c.1339-49C>T r.(=) p.(=) g.48547660C>T Copied from the Exome Variant Server WAS_000052 1/10366 1/6602 0/3764
?/? c.1339-18G>A r.(=) p.(=) g.48547691G>A Copied from the Exome Variant Server WAS_000053 1/10523 1/6709 0/3814
?/? c.1339-3C>T r.spl? p.? g.48547706C>T Copied from the Exome Variant Server WAS_000054 1/10547 1/6716 0/3831
?/? c.1378C>T r.(?) p.(Pro460Ser) g.48547748C>T Copied from the Exome Variant Server WAS_000055 15/10562 13/6727 2/3835
?/? c.1416C>T r.(=) p.(=) g.48547786C>T Copied from the Exome Variant Server WAS_000056 1/10563 0/6728 1/3835
?/? c.1453+16C>T r.(=) p.(=) g.48547839C>T Copied from the Exome Variant Server WAS_000057 19/10556 16/6724 3/3832
?/? c.1454-73G>A r.(=) p.(=) g.48549425G>A Copied from the Exome Variant Server WAS_000058 1/3600 1/2391 0/1209
?/? c.1454-36C>T r.(=) p.(=) g.48549462C>T Copied from the Exome Variant Server WAS_000059 1/10563 0/6728 1/3835
?/? c.1455C>T r.(=) p.(=) g.48549499C>T Copied from the Exome Variant Server WAS_000060 5/10563 0/6728 5/3835
?/? c.1467C>T r.(=) p.(=) g.48549511C>T Copied from the Exome Variant Server WAS_000061 2/10563 0/6728 2/3835
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