All transcript variants in gene SNCG

Information The variants shown are described using the NM_003087.2 transcript reference sequence.

51 entries on 1 page. Showing entries 1 - 51.
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Effect     

AscendingDNA change (cDNA)     

RNA change     

Protein     

DNA change (genomic) (hg19)     

Reference     

DB-ID     

Frequency     

Freq. EA     

Freq. AA     
?/? c.-45T>C r.(=) p.(=) g.88718410T>C Copied from the Exome Variant Server SNCG_000003 1/13006 0/8600 1/4406
?/? c.-31G>A r.(=) p.(=) g.88718424G>A Copied from the Exome Variant Server SNCG_000001 1/13006 1/8600 0/4406
?/? c.-19A>C r.(=) p.(=) g.88718436A>C Copied from the Exome Variant Server SNCG_000002 6891/13006 4634/8600 2257/4406
?/? c.7G>A r.(?) p.(Val3Ile) g.88718461G>A Copied from the Exome Variant Server SNCG_000004 12/13006 0/8600 12/4406
?/? c.30C>A r.(=) p.(=) g.88718484C>A Copied from the Exome Variant Server SNCG_000005 198/13006 3/8600 195/4406
?/? c.50G>A r.(?) p.(Gly17Asp) g.88718504G>A Copied from the Exome Variant Server SNCG_000006 1/13006 0/8600 1/4406
?/? c.54G>A r.(=) p.(=) g.88718508G>A Copied from the Exome Variant Server SNCG_000007 1/13006 1/8600 0/4406
?/? c.114G>A r.(?) p.(Met38Ile) g.88718568G>A Copied from the Exome Variant Server SNCG_000008 3/13006 3/8600 0/4406
?/? c.121+12A>G r.(=) p.(=) g.88718587A>G Copied from the Exome Variant Server SNCG_000009 1/13006 1/8600 0/4406
?/? c.122-53C>T r.(=) p.(=) g.88719337C>T Copied from the Exome Variant Server SNCG_000010 1/4566 0/3182 1/1384
?/? c.122-39C>T r.(=) p.(=) g.88719351C>T Copied from the Exome Variant Server SNCG_000011 2/13006 1/8600 1/4406
?/? c.122-23T>A r.(=) p.(=) g.88719367T>A Copied from the Exome Variant Server SNCG_000012 7/13006 0/8600 7/4406
?/? c.163+31G>A r.(=) p.(=) g.88719462G>A Copied from the Exome Variant Server SNCG_000013 1/13006 1/8600 0/4406
?/? c.164T>C r.(?) p.(Val55Ala) g.88719758T>C Copied from the Exome Variant Server SNCG_000014 16/12984 13/8596 3/4388
?/? c.195C>G r.(=) p.(=) g.88719789C>G Copied from the Exome Variant Server SNCG_000015 3348/13006 2140/8600 1208/4406
?/? c.196G>A r.(?) p.(Val66Met) g.88719790G>A Copied from the Exome Variant Server SNCG_000016 1/13006 1/8600 0/4406
?/? c.220G>A r.(?) p.(Val74Ile) g.88719814G>A Copied from the Exome Variant Server SNCG_000017 3/13006 3/8600 0/4406
?/? c.259A>G r.(?) p.(Asn87Asp) g.88719853A>G Copied from the Exome Variant Server SNCG_000018 1/13006 0/8600 1/4406
?/? c.265G>A r.(?) p.(Ala89Thr) g.88719859G>A Copied from the Exome Variant Server SNCG_000019 19/13004 0/8598 19/4406
?/? c.279G>A r.(=) p.(=) g.88719873G>A Copied from the Exome Variant Server SNCG_000020 128/13006 2/8600 126/4406
?/? c.286C>T r.(?) p.(Arg96Cys) g.88719880C>T Copied from the Exome Variant Server SNCG_000021 1/13006 1/8600 0/4406
?/? c.287G>A r.(?) p.(Arg96His) g.88719881G>A Copied from the Exome Variant Server SNCG_000022 1/13006 0/8600 1/4406
?/? c.291+10G>A r.(=) p.(=) g.88719895G>A Copied from the Exome Variant Server SNCG_000023 24/13004 23/8598 1/4406
?/? c.291+24C>T r.(=) p.(=) g.88719909C>T Copied from the Exome Variant Server SNCG_000024 1/13004 1/8598 0/4406
?/? c.291+43C>A r.(=) p.(=) g.88719928C>A Copied from the Exome Variant Server SNCG_000025 2/13002 1/8596 1/4406
?/? c.292-39T>C r.(=) p.(=) g.88722322T>C Copied from the Exome Variant Server SNCG_000026 1/12996 1/8596 0/4400
?/? c.292-22T>C r.(=) p.(=) g.88722339T>C Copied from the Exome Variant Server SNCG_000027 1/13004 1/8598 0/4406
?/? c.292-16C>T r.(=) p.(=) g.88722345C>T Copied from the Exome Variant Server SNCG_000028 2/13006 0/8600 2/4406
?/? c.292-13T>C r.(=) p.(=) g.88722348T>C Copied from the Exome Variant Server SNCG_000029 1/13006 1/8600 0/4406
?/? c.311C>T r.(?) p.(Ala104Val) g.88722380C>T Copied from the Exome Variant Server SNCG_000030 22/13006 0/8600 22/4406
?/? c.328G>A r.(?) p.(Glu110Lys) g.88722397G>A Copied from the Exome Variant Server SNCG_000031 28/13006 0/8600 28/4406
?/? c.329A>T r.(?) p.(Glu110Val) g.88722398A>T Copied from the Exome Variant Server SNCG_000032 2968/13006 2144/8600 824/4406
?/? c.363+26C>G r.(=) p.(=) g.88722458C>G Copied from the Exome Variant Server SNCG_000033 1/12998 0/8600 1/4398
?/? c.363+29_363+30insG r.(=) p.(=) g.88722461_88722462insG Copied from the Exome Variant Server SNCG_000034 1/12506 1/8248 0/4258
?/? c.363+30G>T r.(=) p.(=) g.88722462G>T Copied from the Exome Variant Server SNCG_000035 190/12994 2/8596 188/4398
?/? c.363+33G>C r.(=) p.(=) g.88722465G>C Copied from the Exome Variant Server SNCG_000036 1/12990 1/8592 0/4398
?/? c.363+38C>T r.(=) p.(=) g.88722470C>T Copied from the Exome Variant Server SNCG_000037 1/12988 1/8592 0/4396
?/? c.363+41T>G r.(=) p.(=) g.88722473T>G Copied from the Exome Variant Server SNCG_000038 1693/12978 645/8586 1048/4392
?/? c.363+66C>T r.(=) p.(=) g.88722498C>T Copied from the Exome Variant Server SNCG_000039 1/4566 0/3182 1/1384
?/? c.364-64C>A r.(=) p.(=) g.88722658C>A Copied from the Exome Variant Server SNCG_000040 514/4566 244/3182 270/1384
?/? c.364-56G>A r.(=) p.(=) g.88722666G>A Copied from the Exome Variant Server SNCG_000041 51/4566 0/3182 51/1384
?/? c.364-53G>A r.(=) p.(=) g.88722669G>A Copied from the Exome Variant Server SNCG_000042 52/4566 0/3182 52/1384
?/? c.364-51C>T r.(=) p.(=) g.88722671C>T Copied from the Exome Variant Server SNCG_000043 11/12982 0/8582 11/4400
?/? c.364-38G>A r.(=) p.(=) g.88722684G>A Copied from the Exome Variant Server SNCG_000044 2/12994 2/8590 0/4404
?/? c.373G>A r.(?) p.(Gly125Arg) g.88722731G>A Copied from the Exome Variant Server SNCG_000045 1/13004 1/8600 0/4404
?/? c.*8C>T r.(=) p.(=) g.88722750C>T Copied from the Exome Variant Server SNCG_000046 1/13000 1/8600 0/4400
?/? c.*12C>A r.(=) p.(=) g.88722754C>A Copied from the Exome Variant Server SNCG_000047 1/13000 0/8600 1/4400
?/? c.*16C>T r.(=) p.(=) g.88722758C>T Copied from the Exome Variant Server SNCG_000048 1/13002 1/8600 0/4402
?/? c.*32A>G r.(=) p.(=) g.88722774A>G Copied from the Exome Variant Server SNCG_000049 122/13002 2/8598 120/4404
?/? c.*34C>T r.(=) p.(=) g.88722776C>T Copied from the Exome Variant Server SNCG_000050 218/13002 39/8598 179/4404
?/? c.*35G>A r.(=) p.(=) g.88722777G>A Copied from the Exome Variant Server SNCG_000051 5/13002 5/8598 0/4404
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