Transcript #00004292 (NM_001141970.1, DAXX gene)

Transcript name transcript variant 3
Gene name DAXX (death-domain associated protein)
Chromosome 6
Transcript - NCBI ID NM_001141970.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001135442.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

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

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/? c.-61_-60del r.(=) p.(=)
?/? c.-47C>T r.(=) p.(=)
?/? c.-32C>T r.(=) p.(=)
?/? c.-25A>T r.(=) p.(=)
?/? c.-23T>C r.(=) p.(=)
?/? c.-8A>C r.(=) p.(=)
?/? c.20G>C r.(?) p.(Cys7Ser)
?/? c.50T>C r.(?) p.(Leu17Pro)
?/? c.53+7G>C r.(=) p.(=)
?/? c.53+26A>C r.(=) p.(=)
?/? c.54-46C>T r.(=) p.(=)
?/? c.70G>A r.(?) p.(Asp24Asn)
?/? c.94G>A r.(?) p.(Ala32Thr)
?/? c.342G>A r.(=) p.(=)
?/? c.344C>T r.(?) p.(Ala115Val)
?/? c.384C>T r.(=) p.(=)
?/? c.405C>A r.(=) p.(=)
?/? c.419A>G r.(?) p.(Asn140Ser)
?/? c.421G>A r.(?) p.(Glu141Lys)
?/? c.437T>C r.(?) p.(Leu146Pro)
?/? c.468C>T r.(=) p.(=)
?/? c.480C>T r.(=) p.(=)
?/? c.487A>G r.(?) p.(Thr163Ala)
?/? c.488C>T r.(?) p.(Thr163Ile)
?/? c.516T>G r.(=) p.(=)
?/? c.543A>G r.(=) p.(=)
?/? c.571C>T r.(?) p.(Pro191Ser)
?/? c.593G>A r.(?) p.(Arg198Gln)
?/? c.636A>C r.(=) p.(=)
?/? c.654G>A r.(=) p.(=)
?/? c.661G>A r.(?) p.(Glu221Lys)
?/? c.783C>T r.(=) p.(=)
?/? c.798G>A r.(=) p.(=)
?/? c.844C>T r.(?) p.(Arg282Cys)
?/? c.867G>C r.(?) p.(Lys289Asn)
?/? c.953G>A r.(?) p.(Arg318Gln)
?/? c.1063G>C r.(?) p.(Asp355His)
?/? c.1075+7G>T r.(=) p.(=)
?/? c.1075+47A>G r.(=) p.(=)
?/? c.1076-40T>G r.(=) p.(=)
?/? c.1076-22G>A r.(=) p.(=)
?/? c.1076-4G>A r.spl? p.?
?/? c.1089A>G r.(=) p.(=)
?/? c.1094C>T r.(?) p.(Ser365Leu)
?/? c.1111C>T r.(?) p.(Arg371Trp)
?/? c.1114C>T r.(?) p.(Arg372Cys)
?/? c.1116C>A r.(=) p.(=)
?/? c.1159G>A r.(?) p.(Val387Ile)
?/? c.1169A>G r.(?) p.(Lys390Arg)
?/? c.1173T>C r.(=) p.(=)
?/? c.1174G>A r.(?) p.(Ala392Thr)
?/? c.1209A>G r.(=) p.(=)
?/? c.1250C>G r.(?) p.(Ser417Cys)
?/? c.1252G>C r.(?) p.(Ala418Pro)
?/? c.1287+43C>G r.(=) p.(=)
?/? c.1288-40G>A r.(=) p.(=)
?/? c.1288-20G>A r.(=) p.(=)
?/? c.1300A>G r.(?) p.(Met434Val)
?/? c.1301T>C r.(?) p.(Met434Thr)
?/? c.1350_1352del r.(?) p.(Glu450del)
?/? c.1353C>T r.(=) p.(=)
?/? c.1354G>A r.(?) p.(Asp452Asn)
?/? c.1356_1358del r.(?) p.(Asp452del)
?/? c.1360_1362del r.(?) p.(Glu454del)
?/? c.1374_1379del r.(?) p.(Glu468_Glu469del)
?/? c.1386_1388del r.(?) p.(Glu469del)
?/? c.1386_1391del r.(?) p.(Glu468_Glu469del)
?/? c.1406_1408del r.(?) p.(Glu469del)
?/? c.1431_1433del r.(?) p.(Glu477del)
?/? c.1467T>C r.(=) p.(=)
?/? c.1470_1472del r.(?) p.(Glu492del)
?/? c.1479C>T r.(=) p.(=)
?/? c.1480G>A r.(?) p.(Glu494Lys)
?/? c.1493C>G r.(?) p.(Ala498Gly)
?/? c.1501+10G>A r.(=) p.(=)
?/? c.1547A>G r.(?) p.(Asn516Ser)
?/? c.1606A>G r.(?) p.(Lys536Glu)
?/? c.1613G>A r.(?) p.(Arg538His)
?/? c.1623_1628del r.(?) p.(Pro542_Ser543del)
?/? c.1629G>A r.(=) p.(=)
?/? c.1693G>A r.(?) p.(Glu565Lys)
?/? c.1787C>T r.(?) p.(Thr596Met)
?/? c.1841A>C r.(?) p.(Glu614Ala)
?/? c.1885G>A r.(?) p.(Val629Ile)
?/? c.1935G>A r.(=) p.(=)
?/? c.1950A>G r.(=) p.(=)
?/? c.1976+42T>C r.(=) p.(=)
?/? c.1977-33T>C r.(=) p.(=)
?/? c.2024T>A r.(?) p.(Ile675Lys)
?/? c.2050C>T r.(?) p.(Pro684Ser)
?/? c.2067C>A r.(=) p.(=)
?/? c.2128C>T r.(?) p.(Leu710Phe)
?/? c.2130C>G r.(=) p.(=)
?/? c.2148C>T r.(=) p.(=)
?/? c.2150G>T r.(?) p.(Arg717Leu)
?/? c.2153T>A r.(?) p.(Leu718Gln)
?/? c.2154G>A r.(=) p.(=)
?/? c.2182C>T r.(?) p.(Arg728Trp)
?/? c.2196C>T r.(=) p.(=)
?/? c.2199+16C>T r.(=) p.(=)
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