Transcript #00013814

Transcript name transcript variant 2
Gene name PALLD (palladin, cytoskeletal associated protein)
Chromosome 4
Transcript - NCBI ID NM_016081.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_057165.3
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

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

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/? c.-20T>C r.(=) p.(=)
?/? c.-8G>A r.(=) p.(=)
?/? c.-7T>C r.(=) p.(=)
?/? c.8G>T r.(?) p.(Gly3Val)
?/? c.18C>T r.(=) p.(=)
?/? c.83C>T r.(?) p.(Pro28Leu)
?/? c.84G>A r.(=) p.(=)
?/? c.116T>A r.(?) p.(Ile39Lys)
?/? c.140G>A r.(?) p.(Arg47Gln)
?/? c.149T>C r.(?) p.(Ile50Thr)
?/? c.186G>A r.(=) p.(=)
?/? c.195G>A r.(=) p.(=)
?/? c.223C>T r.(?) p.(Leu75Phe)
?/? c.229G>C r.(?) p.(Glu77Gln)
?/? c.232C>T r.(?) p.(His78Tyr)
?/? c.250A>C r.(?) p.(Thr84Pro)
?/? c.267C>A r.(?) p.(His89Gln)
?/? c.275G>C r.(?) p.(Arg92Thr)
?/? c.306C>T r.(=) p.(=)
?/? c.331A>G r.(?) p.(Lys111Glu)
?/? c.365C>T r.(?) p.(Pro122Leu)
?/? c.366T>G r.(=) p.(=)
?/? c.399C>T r.(=) p.(=)
?/? c.401T>A r.(?) p.(Ile134Asn)
?/? c.413G>A r.(?) p.(Arg138Gln)
?/? c.428G>A r.(?) p.(Arg143His)
?/? c.453C>T r.(=) p.(=)
?/? c.460C>A r.(?) p.(Pro154Thr)
?/? c.467C>T r.(?) p.(Thr156Met)
?/? c.468G>A r.(=) p.(=)
?/? c.481A>C r.(?) p.(Lys161Gln)
?/? c.492C>T r.(=) p.(=)
?/? c.502C>G r.(?) p.(Leu168Val)
?/? c.539C>T r.(?) p.(Thr180Ile)
?/? c.556G>A r.(?) p.(Ala186Thr)
?/? c.594G>A r.(=) p.(=)
?/? c.671T>C r.(?) p.(Met224Thr)
?/? c.672G>A r.(?) p.(Met224Ile)
?/? c.678C>T r.(=) p.(=)
?/? c.723T>A r.(?) p.(His241Gln)
?/? c.729C>T r.(=) p.(=)
?/? c.730C>T r.(?) p.(Gln244*)
?/? c.731A>G r.(?) p.(Gln244Arg)
?/? c.764G>A r.(?) p.(Arg255His)
?/? c.789C>T r.(=) p.(=)
?/? c.815G>A r.(?) p.(Arg272Gln)
?/? c.856A>G r.(?) p.(Ser286Gly)
?/? c.859C>T r.(?) p.(Arg287*)
?/? c.860G>A r.(?) p.(Arg287Gln)
?/? c.902G>A r.(?) p.(Arg301Gln)
?/? c.908+6A>C r.(=) p.(=)
?/? c.909A>T r.(?) p.(Arg303Ser)
?/? c.910T>C r.(?) p.(Trp304Arg)
?/? c.970G>T r.(?) p.(Gly324Trp)
?/? c.972G>A r.(=) p.(=)
?/? c.1012G>A r.(?) p.(Asp338Asn)
?/? c.1022G>A r.(?) p.(Arg341His)
?/? c.1040C>T r.(?) p.(Thr347Met)
?/? c.1059_1060insACA r.(?) p.(Thr355dup)
?/? c.1082T>C r.(?) p.(Ile361Thr)
?/? c.1087+9G>A r.(=) p.(=)
?/? c.1087+24G>C r.(=) p.(=)
?/? c.1087+27G>T r.(=) p.(=)
?/? c.1088-10A>C r.(=) p.(=)
?/? c.1129A>G r.(?) p.(Lys377Glu)
?/? c.1154+11A>G r.(=) p.(=)
?/? c.1154+46A>T r.(=) p.(=)
?/? c.1155-49A>G r.(=) p.(=)
?/? c.1155-47G>A r.(=) p.(=)
?/? c.1155-21A>C r.(=) p.(=)
?/? c.1155-19T>C r.(=) p.(=)
?/? c.1155-9A>G r.(=) p.(=)
?/? c.1240C>T r.(=) p.(=)
?/? c.1260+35C>A r.(=) p.(=)
?/? c.1261-11T>G r.(=) p.(=)
?/? c.1266C>G r.(?) p.(His422Gln)
?/? c.1273A>T r.(?) p.(Thr425Ser)
?/? c.1274C>A r.(?) p.(Thr425Asn)
?/? c.1289G>A r.(?) p.(Arg430Gln)
?/? c.1297G>A r.(?) p.(Gly433Arg)
?/? c.1301C>T r.(?) p.(Thr434Ile)
?/? c.1335+58C>T r.(=) p.(=)
?/? c.1336-44A>G r.(=) p.(=)
?/? c.1336-42C>G r.(=) p.(=)
?/? c.1336-41A>G r.(=) p.(=)
?/? c.1336-23C>T r.(=) p.(=)
?/? c.1336-10T>C r.(=) p.(=)
?/? c.1347C>T r.(=) p.(=)
?/? c.1358C>T r.(?) p.(Ala453Val)
?/? c.1372G>A r.(?) p.(Val458Met)
?/? c.1374G>A r.(=) p.(=)
?/? c.1380G>C r.(=) p.(=)
?/? c.1394G>A r.(?) p.(Arg465His)
?/? c.1477+16C>T r.(=) p.(=)
?/? c.1477+31G>A r.(=) p.(=)
?/? c.1478-70_1478-69insT r.(=) p.(=)
?/? c.1501+35_1501+36insG r.(=) p.(=)
?/? c.1501+43C>A r.(=) p.(=)
?/? c.1501+85C>T r.(=) p.(=)
?/? c.1502-25A>C r.(=) p.(=)
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