Transcript #00023886 (NM_006096.3, NDRG1 gene)

Transcript name transcript variant 2
Gene name NDRG1 (N-myc downstream regulated 1)
Chromosome 8
Transcript - NCBI ID NM_006096.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_006087.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2013-11-25 18:38:36 +01:00 (CET)
Date last edited N/A


Variants

86 entries on 1 page. Showing entries 1 - 86.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-/. - c.-19+49C>T r.(?) p.(=)
-?/. - c.-18-2_-18-1del r.spl? p.?
-?/. - c.31G>A r.(?) p.(Ala11Thr)
-?/. - c.31G>A r.(?) p.(Ala11Thr)
-/. - c.64-6T>C r.(=) p.(=)
-/. - c.64-6T>C r.(=) p.(=)
-/. - c.64-6T>C r.= p.=
-/. - c.64-6T>C r.(=) p.(=)
-?/. - c.72C>T r.(?) p.(=)
?/. - c.122A>G r.(?) p.(His41Arg)
-?/. - c.135C>T r.(?) p.(His45=)
?/. - c.158A>G r.(?) p.(Lys53Arg)
?/. - c.167G>A r.(?) p.(Arg56Gln)
-/. - c.199A>G r.(?) p.(Met67Val)
+?/. - c.237C>A r.(?) p.(Tyr79Ter)
-/. - c.306C>T r.(?) p.(Gly102=)
-?/. - c.321C>T r.(?) p.(=)
-/. - c.326+64G>C r.(?) p.?
-/. - c.327-48C>G r.(=) p.(=)
?/. - c.331A>C r.(?) p.(Met111Leu)
-?/. - c.389+13G>C r.(=) p.(=)
+/. 6i_9i c.389+93_594+1641dup r.390_594dup Glu199AlafsTer25
+/. 6i_9i c.389+93_594+1641dup r.390_594dup Glu199AlafsTer25
+/. 6i_9i c.389+93_594+1641dup r.390_594dup Glu199AlafsTer25
+?/. 7 c.437T>C r.(?) p.(Leu146Pro)
+/. - c.442C>T r.(?) p.(Arg148*)
+/. - c.442C>T r.(?) p.(Arg148Ter)
+/. - c.442C>T r.(?) p.(Arg148*)
+/. - c.442C>T r.(?) p.(Arg148*)
+/. - c.442C>T r.(?) p.(Arg148Ter)
+/. - c.442C>T r.(?) p.(Arg148Ter)
+/. - c.442C>T r.(?) p.(Arg148Ter)
+/. - c.442C>T r.(?) p.(Arg148Ter)
+/. - c.442C>T r.(?) p.(Arg148Ter)
+/. - c.442C>T r.(?) p.(Arg148Ter)
+/. - c.442C>T r.(?) p.(Arg148Ter)
+/. - c.442C>T r.(?) p.(Arg148Ter)
+/. - c.442C>T r.(?) p.(Arg148Ter)
+/. 7 c.442C>T r.(?) p.(Arg148Ter)
?/. - c.448G>A r.(?) p.(Ala150Thr)
-?/. - c.450+20T>C r.(=) p.(=)
?/. - c.450+139_450+140del r.(=) p.(=)
-/. - c.450+152C>T r.(=) p.(=)
+/. 8i c.451-1G>A r.451_537del p.Leu151_Lys179del
-/. - c.507G>A r.(?) p.(Ala169=)
+?/. - c.516G>A r.(?) p.(Trp172Ter)
+/. - c.538-1G>A r.spl? p.?
?/. - c.563C>T r.(?) p.(Pro188Leu)
-?/. - c.595-17C>T r.(=) p.(=)
?/. - c.613G>A r.(?) p.(Val205Met)
-?/. - c.686A>G r.(?) p.(Asn229Ser)
-/. - c.698+77G>A r.(?) p.?
-/. - c.698+84A>G r.(?) p.?
-/. - c.699-51A>C r.(?) p.?
-/. - c.699-16C>G r.(=) p.(=)
+?/. 11 c.701G>A r.(?) p.(Arg234Gln)
?/. - c.703C>T r.(?) p.(Arg235Cys)
?/. - c.731C>G r.(?) p.(Pro244Arg)
-/. - c.755+10T>C r.(=) p.(=)
-/. - c.755+10T>C r.= p.=
-/. - c.755+10T>C r.(=) p.(=)
-/. - c.756-5C>T r.(=) p.(=)
-/. - c.756-5C>T r.spl? p.?
-/. - c.756-5C>T r.= p.=
?/. - c.779_780insTGCACCTGT r.(?) p.(Gly260_Asp261insAlaProVal)
-?/. - c.789G>A r.(?) p.(Ser263=)
-?/. - c.789G>A r.(?) p.(Ser263=)
-/. - c.855+148T>C r.(?) p.?
-?/. - c.856-19G>A r.(=) p.(=)
-?/. - c.879G>A r.(?) p.(Pro293=)
-/. - c.891+39C>A r.(=) p.(=)
-/. - c.891+39C>T r.(?) p.?
-/. - c.892-5C>T r.spl? p.?
-?/. - c.894G>A r.(?) p.(=)
?/. - c.899A>G r.(?) p.(Lys300Arg)
-/. - c.944-91C>T r.(?) p.?
-/. - c.944-90G>A r.(?) p.?
-?/. - c.944-13C>T r.(=) p.(=)
+/. - c.944-1G>T r.spl? p.?
+?/. - c.948del r.(?) p.(Ser317Argfs*4)
?/. - c.965G>A r.(?) p.(Arg322His)
-?/. - c.973C>A r.(?) p.(Arg325=)
?/. - c.973C>T r.(?) p.(Arg325Trp)
?/. - c.1088G>A r.(?) p.(Arg363His)
-?/. - c.1092G>A r.(?) p.(Ser364=)
-?/. - c.1155C>T r.(?) p.(Ala385=)
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