Transcript #00000419

Transcript name angiogenic factor with G patch and FHA domains 1
Gene name AGGF1 (angiogenic factor with G patch and FHA domains 1)
Chromosome 5
Transcript - NCBI ID NM_018046.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_060516.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

114 entries on 2 pages. Showing entries 1 - 100.
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Affects function     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/? c.-48C>T r.(=) p.(=)
?/? c.35C>T r.(?) p.(Pro12Leu)
?/? c.50C>T r.(?) p.(Ser17Phe)
?/? c.52C>G r.(?) p.(Pro18Ala)
?/? c.55G>T r.(?) p.(Glu19*)
?/? c.59C>T r.(?) p.(Pro20Leu)
?/? c.84G>A r.(=) p.(=)
?/? c.140A>G r.(?) p.(Glu47Gly)
?/? c.157A>G r.(?) p.(Thr53Ala)
?/? c.163C>T r.(?) p.(Arg55Trp)
?/? c.207G>A r.(=) p.(=)
?/? c.210+26C>A r.(=) p.(=)
?/? c.211-45G>C r.(=) p.(=)
?/? c.266C>T r.(?) p.(Ser89Phe)
?/? c.307A>G r.(?) p.(Ile103Val)
?/? c.313+6T>C r.(=) p.(=)
?/? c.313+11T>C r.(=) p.(=)
?/? c.313+43A>G r.(=) p.(=)
?/? c.314-3C>T r.spl? p.?
?/? c.329C>T r.(?) p.(Thr110Met)
?/? c.335A>G r.(?) p.(Tyr112Cys)
?/? c.367G>A r.(?) p.(Glu123Lys)
?/? c.397G>A r.(?) p.(Glu133Lys)
?/? c.399A>G r.(=) p.(=)
?/? c.459C>T r.(=) p.(=)
?/? c.517-46_517-45insA r.(=) p.(=)
?/? c.517-24T>C r.(=) p.(=)
?/? c.529G>A r.(?) p.(Ala177Thr)
?/? c.612G>C r.(?) p.(Gln204His)
?/? c.629A>T r.(?) p.(Asp210Val)
?/? c.682-42A>G r.(=) p.(=)
?/? c.682-22A>G r.(=) p.(=)
?/? c.703C>A r.(?) p.(Pro235Thr)
?/? c.733G>A r.(?) p.(Val245Met)
?/? c.763C>T r.(?) p.(Arg255*)
?/? c.813T>A r.(?) p.(Asp271Glu)
?/? c.844G>T r.(?) p.(Asp282Tyr)
?/? c.870G>T r.(?) p.(Lys290Asn)
?/? c.870+26T>G r.(=) p.(=)
?/? c.870+48_870+51del r.(=) p.(=)
?/? c.871-42G>A r.(=) p.(=)
?/? c.871-31del r.(=) p.(=)
?/? c.871-30G>C r.(=) p.(=)
?/? c.871-19T>A r.(=) p.(=)
?/? c.871-10C>G r.(=) p.(=)
?/? c.878A>G r.(?) p.(Asn293Ser)
?/? c.939C>T r.(=) p.(=)
?/? c.940G>T r.(?) p.(Ala314Ser)
?/? c.947T>A r.(?) p.(Met316Lys)
?/? c.978C>T r.(=) p.(=)
?/? c.1024A>G r.(?) p.(Ile342Val)
?/? c.1048A>T r.(?) p.(Ile350Phe)
?/? c.1145A>G r.(?) p.(Tyr382Cys)
?/? c.1146T>C r.(=) p.(=)
?/? c.1149C>T r.(=) p.(=)
?/? c.1178C>T r.(?) p.(Thr393Ile)
?/? c.1188T>C r.(=) p.(=)
?/? c.1201+19T>C r.(=) p.(=)
?/? c.1202-32A>G r.(=) p.(=)
?/? c.1202-25A>G r.(=) p.(=)
?/? c.1211A>G r.(?) p.(Lys404Arg)
?/? c.1215T>C r.(=) p.(=)
?/? c.1221C>T r.(=) p.(=)
?/? c.1313+8G>A r.(=) p.(=)
?/? c.1313+25C>T r.(=) p.(=)
?/? c.1313+45A>C r.(=) p.(=)
?/? c.1339C>T r.(?) p.(Arg447*)
?/? c.1365+31C>T r.(=) p.(=)
?/? c.1365+49_1365+51del r.(=) p.(=)
?/? c.1366-50T>C r.(=) p.(=)
?/? c.1366-8del r.(=) p.(=)
?/? c.1368T>G r.(?) p.(Phe456Leu)
?/? c.1395C>T r.(=) p.(=)
?/? c.1410C>T r.(=) p.(=)
?/? c.1467+38del r.(=) p.(=)
?/? c.1467+47T>C r.(=) p.(=)
?/? c.1467+49_1467+50insT r.(=) p.(=)
?/? c.1468-47A>G r.(=) p.(=)
?/? c.1468-43G>A r.(=) p.(=)
?/? c.1468-6C>T r.(=) p.(=)
?/? c.1492G>A r.(?) p.(Val498Ile)
?/? c.1566C>T r.(=) p.(=)
?/? c.1578T>C r.(=) p.(=)
?/? c.1622A>G r.(?) p.(Asp541Gly)
?/? c.1629T>C r.(=) p.(=)
?/? c.1633+40_1633+43del r.(=) p.(=)
?/? c.1633+51C>G r.(=) p.(=)
?/? c.1634-31C>A r.(=) p.(=)
?/? c.1716+34C>G r.(=) p.(=)
?/? c.1717-49_1717-46del r.(=) p.(=)
?/? c.1744T>G r.(?) p.(Leu582Val)
?/? c.1800T>A r.(?) p.(Ser600Arg)
?/? c.1820A>T r.(?) p.(Asp607Val)
?/? c.1844C>T r.(?) p.(Ser615Phe)
?/? c.1844+45T>C r.(=) p.(=)
?/? c.1845-38C>G r.(=) p.(=)
?/? c.1845-4A>G r.spl? p.?
?/? c.1862A>G r.(?) p.(Asn621Ser)
?/? c.1870C>T r.(?) p.(Arg624Trp)
?/? c.1890G>A r.(?) p.(Met630Ile)
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