Transcript #00021553 (NM_003844.3, TNFRSF10A gene)

Transcript name tumor necrosis factor receptor superfamily, member 10a
Gene name TNFRSF10A (tumor necrosis factor receptor superfamily, member 10a)
Chromosome 8
Transcript - NCBI ID NM_003844.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_003835.3
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

77 entries on 1 page. Showing entries 1 - 77.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Predict-BioInf     
?/? 1 c.32G>T r.(?) c.(Gly11Val) -
?/? 1 c.98C>T r.(?) p.(Thr33Ile) -
?/? 1 c.206G>C r.(?) p.(Arg69Pro) -
?/? 1 c.227C>T r.(?) p.(Pro76Leu) -
?/? 1i c.306+5G>C r.spl? p.(?) -
?/? 2 c.314C>G r.(?) p.(Pro105Arg) Polyphen: possibly damaging
?/? 2 c.328A>G r.(?) p.(Thr110Ala) Polyphen: benign
?/? 2 c.341A>G r.(?) p.(His114Arg) -
?/? 2 c.370dup r.(?) p.(Glu124Glyfs*3) -
?/? 2 c.397C>T r.(?) p.(Pro133Ser) Polyphen: probably damaging
?/? 3 c.422A>G r.(?) p.(His141Arg) Polyphen: possibly damaging
?/? 3 c.422A>G r.(?) p.(His141Arg) Polyphen: possibly damaging
?/? 3 c.422A>G r.(?) p.(His141Arg) Polyphen: possibly damaging
?/? 3 c.465C>A r.(?) p.(=) -
?/? 3i c.517+6G>C r.(?) p.(=) -
?/? 4 c.587G>A r.(?) p.(Arg196Gln) -
?/? 4 c.613C>T r.(?) p.(Arg205Trp) Polyphen: probably damaging
?/? 4 c.626G>C r.(?) p.(Arg209Thr) Polyphen: benign
?/? 4 c.626G>C r.(?) p.(Arg209Thr) Polyphen: benign
?/? 4 c.626G>C r.(?) p.(Arg209Thr) Polyphen: benign
?/? 4 c.626G>C r.(?) p.(Arg209Thr) Polyphen: benign
?/? 4 c.626G>C r.(?) p.(Arg209Thr) Polyphen: benign
?/? 4 c.626G>C r.(?) p.(Arg209Thr) Polyphen: benign
?/? 4 c.626G>C r.(?) p.(Arg209Thr) Polyphen: benign
?/? 4 c.626G>C r.(?) p.(Arg209Thr) Polyphen: benign
?/? 5 c.633C>G r.(?) p.(Cys211Trp) -
?/? 5 c.652G>T r.(?) p.(Val218Phe) Polyphen: probably damaging
?/? 5 c.659A>G r.(?) p.(Asp220Gly) -
?/? 5 c.683A>C r.(?) p.(Glu228Ala) Polyphen: possibly damaging
?/? 5 c.683A>C r.(?) p.(Glu228Ala) Polyphen: possibly damaging
?/? 5 c.683A>C r.(?) p.(Glu228Ala) Polyphen: possibly damaging
?/? 5 c.683A>C r.(?) p.(Glu228Ala) Polyphen: possibly damaging
?/? 5 c.683A>C r.(?) p.(Glu228Ala) Polyphen: possibly damaging
?/? 5 c.683A>C r.(?) p.(Glu228Ala) Polyphen: possibly damaging
?/? 6 c.736G>T r.(?) p.(Val246Leu) -
?/? 8 c.837T>A r.(?) p.(Cys279*) -
?/? 8 c.845G>A r.(?) p.(Arg282His) -
?/? 8 c.854T>A r.(?) p.(Leu285His) -
?/? 8 c.859C>T r.(?) p.(Arg287*) -
?/? 8 c.865C>T r.(?) p.(Pro289Ser) Polyphen: probably damaging
?/? 8 c.889A>C r.(?) p.(Asn297His) Polyphen: probably damaging
?/? 8 c.891C>T r.(?) p.(=) -
?/? 8 c.906C>T r.(?) p.(=) -
?/? 8 c.956A>G r.(?) p.(Glu319Gly) -
?/? 8 c.959C>T r.(?) p.(Pro320Leu) Polyphen: probably damaging
?/? 8 c.976G>A r.(?) p.(Val326Ile) -
?/? 8 c.999G>A r.(?) p.(=) -
?/? 9 c.1019C>T r.(?) p.(Pro340Leu) Polyphen: probably damaging
?/? 9 c.1070G>A r.(?) p.(Gly357Asp) -
?/? 9 c.1086G>T r.(?) p.(Glu362Asp) Polyphen: possibly damaging
?/? 9i c.1087+7G>A r.(?) p.(=) -
?/? 10 c.1117A>G r.(?) p.(Asn373Asp) -
?/? 10 c.1127C>T r.(?) p.(Pro376Leu) -
?/? 10 c.1127C>T r.(?) p.(Pro376Leu) -
?/? 10 c.1135T>C r.(?) p.(Ser379Pro) Polyphen: probably damaging
?/? 10 c.1205C>T r.(?) p.(Ala402Val) -
?/? 10 c.1209C>T r.(?) p.(=) -
?/? 10 c.1232T>C r.(?) p.(Met411Thr) Polyphen: probably damaging
?/? 10 c.1245G>T r.(?) p.(Trp415Cys) Polyphen: probably damaging
?/? 10 c.1271C>T r.(?) p.(Ser424Leu) -
?/? 10 c.1283T>C r.(?) p.(Leu428Pro) Polyphen: probably damaging
?/? 10 c.1288G>A r.(?) p.(Asp430Asn) Polyphen: probably damaging
?/? 10 c.1300A>C r.(?) p.(=) -
?/? 10 c.1322G>A r.(?) p.(Arg441Lys) Polyphen: benign
?/? 10 c.1322G>A r.(?) p.(Arg441Lys) Polyphen: benign
?/? 10 c.1322G>A r.(?) p.(Arg441Lys) Polyphen: benign
?/? 10 c.1322G>A r.(?) p.(Arg441Lys) Polyphen: benign
?/? 10 c.1322G>A r.(?) p.(Arg441Lys) Polyphen: benign
?/? 10 c.1322G>A r.(?) p.(Arg441Lys) Polyphen: benign
?/? 10 c.1322G>A r.(?) p.(Arg441Lys) Polyphen: benign
?/? 10 c.1341C>G r.(?) p.(=) -
?/? 10 c.1384G>A r.(?) p.(Gly462Ser) Polyphen: probably damaging
?/? 10 c.1406G>T r.(?) p.(*469Leuext*15) -
?/? 10 c.*59T>G r.(?) p.(=) -
?/? 10 c.*70del r.(?) p.(=) -
?/? 10 c.*70dup r.(?) p.(=) -
?/? 10 c.*197T>G r.(?) p.(=) -
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