Transcript #00000030

Transcript name apoptosis antagonizing transcription factor
Gene name AATF (apoptosis antagonizing transcription factor)
Chromosome 17
Transcript - NCBI ID NM_012138.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_036270.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

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

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/? c.-18G>C r.(=) p.(=)
?/? c.-15C>T r.(=) p.(=)
?/? c.31C>T r.(=) p.(=)
?/? c.126A>G r.(=) p.(=)
?/? c.130G>A r.(?) p.(Glu44Lys)
?/? c.137G>A r.(?) p.(Gly46Glu)
?/? c.169A>G r.(?) p.(Arg57Gly)
?/? c.194T>G r.(?) p.(Leu65Trp)
?/? c.204C>T r.(=) p.(=)
?/? c.237A>G r.(=) p.(=)
?/? c.246T>C r.(=) p.(=)
?/? c.250G>A r.(?) p.(Asp84Asn)
?/? c.253C>T r.(?) p.(His85Tyr)
?/? c.263A>G r.(?) p.(Gln88Arg)
?/? c.271C>A r.(?) p.(Pro91Thr)
?/? c.283+25_283+29del r.(=) p.(=)
?/? c.284A>G r.(?) p.(Asp95Gly)
?/? c.293T>C r.(?) p.(Ile98Thr)
?/? c.332G>A r.(?) p.(Gly111Glu)
?/? c.360C>T r.(=) p.(=)
?/? c.361G>A r.(?) p.(Asp121Asn)
?/? c.420A>G r.(=) p.(=)
?/? c.440C>T r.(?) p.(Pro147Leu)
?/? c.441G>A r.(=) p.(=)
?/? c.490A>G r.(?) p.(Met164Val)
?/? c.520G>A r.(?) p.(Glu174Lys)
?/? c.533G>A r.(?) p.(Ser178Asn)
?/? c.538A>G r.(?) p.(Met180Val)
?/? c.555C>T r.(=) p.(=)
?/? c.557C>T r.(?) p.(Ala186Val)
?/? c.558G>A r.(=) p.(=)
?/? c.568C>T r.(?) p.(Gln190*)
?/? c.588C>T r.(=) p.(=)
?/? c.655G>T r.(?) p.(Glu219*)
?/? c.664G>A r.(?) p.(Glu222Lys)
?/? c.694+23T>G r.(=) p.(=)
?/? c.694+35A>C r.(=) p.(=)
?/? c.694+48T>G r.(=) p.(=)
?/? c.699G>T r.(=) p.(=)
?/? c.728A>G r.(?) p.(Lys243Arg)
?/? c.739G>T r.(?) p.(Ala247Ser)
?/? c.832+7A>C r.(=) p.(=)
?/? c.832+9A>G r.(=) p.(=)
?/? c.832+14T>C r.(=) p.(=)
?/? c.832+30T>C r.(=) p.(=)
?/? c.832+39C>T r.(=) p.(=)
?/? c.832+49T>C r.(=) p.(=)
?/? c.846T>C r.(=) p.(=)
?/? c.923A>G r.(?) p.(Asp308Gly)
?/? c.947+7G>T r.(=) p.(=)
?/? c.947+11A>G r.(=) p.(=)
?/? c.947+18T>C r.(=) p.(=)
?/? c.947+46A>G r.(=) p.(=)
?/? c.976C>T r.(=) p.(=)
?/? c.991A>C r.(?) p.(Lys331Gln)
?/? c.1000C>T r.(?) p.(Arg334*)
?/? c.1001G>A r.(?) p.(Arg334Gln)
?/? c.1022G>A r.(?) p.(Arg341Lys)
?/? c.1039G>A r.(?) p.(Asp347Asn)
?/? c.1064G>A r.(?) p.(Arg355His)
?/? c.1110G>A r.(?) p.(Trp370*)
?/? c.1114G>A r.(?) p.(Asp372Asn)
?/? c.1126C>G r.(?) p.(Leu376Val)
?/? c.1149+11G>A r.(=) p.(=)
?/? c.1149+18C>T r.(=) p.(=)
?/? c.1149+19G>A r.(=) p.(=)
?/? c.1149+41G>A r.(=) p.(=)
?/? c.1150-47C>T r.(=) p.(=)
?/? c.1150-10G>A r.(=) p.(=)
?/? c.1150-1G>A r.spl? p.?
?/? c.1189G>A r.(?) p.(Asp397Asn)
?/? c.1195A>G r.(?) p.(Ile399Val)
?/? c.1222C>T r.(?) p.(Arg408*)
?/? c.1223G>A r.(?) p.(Arg408Gln)
?/? c.1230A>T r.(=) p.(=)
?/? c.1245T>C r.(=) p.(=)
?/? c.1253G>C r.(?) p.(Arg418Pro)
?/? c.1288G>C r.(?) p.(Val430Leu)
?/? c.1313C>T r.(?) p.(Pro438Leu)
?/? c.1314+2T>G r.spl? p.?
?/? c.1314+10C>T r.(=) p.(=)
?/? c.1314+44A>G r.(=) p.(=)
?/? c.1315-37T>C r.(=) p.(=)
?/? c.1315-34G>T r.(=) p.(=)
?/? c.1315-13A>G r.(=) p.(=)
?/? c.1315-13_1315-12insT r.(=) p.(=)
?/? c.1315-4A>G r.spl? p.?
?/? c.1344T>C r.(=) p.(=)
?/? c.1361A>G r.(?) p.(Asp454Gly)
?/? c.1398+16T>A r.(=) p.(=)
?/? c.1398+20_1398+21del r.(=) p.(=)
?/? c.1398+33T>C r.(=) p.(=)
?/? c.1399-39A>G r.(=) p.(=)
?/? c.1399-23C>T r.(=) p.(=)
?/? c.1399C>T r.(?) p.(Leu467Phe)
?/? c.1406G>A r.(?) p.(Arg469Gln)
?/? c.1410A>G r.(=) p.(=)
?/? c.1421del r.(?) p.(Lys475Argfs*31)
?/? c.1446C>T r.(=) p.(=)
?/? c.1447G>A r.(?) p.(Asp483Asn)
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