Transcript #00016670 (NM_001164539.1, DISC1 gene)

Transcript name Manually created transcript. (removed from reference sequence)
Gene name DISC1 (disrupted in schizophrenia 1)
Chromosome 1
Transcript - NCBI ID NM_001164539.1
Transcript - Ensembl ID -
Protein - NCBI ID -
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

67 entries on 1 page. Showing entries 1 - 67.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

Position     

RNA change     

Protein     

PolyPhen prediction     

GVS function     

Splice distance     
./. - c.-7G>A -7 r.(=) p.(=) - utr-5 -
./. - c.-7G>A -7 r.(=) p.(=) - utr-5 -
./. - c.-7G>A -7 r.(=) p.(=) - utr-5 -
./. - c.-7G>A -7 r.(=) p.(=) - utr-5 -
./. - c.-7G>A -7 r.(=) p.(=) - utr-5 -
./. - c.211G>T 211 r.(?) p.(Val71Leu) - missense -
./. - c.211G>T 211 r.(?) p.(Val71Leu) - missense -
./. - c.248C>T 248 r.(?) p.(Ala83Val) - missense -
./. - c.791G>A 791 r.(?) p.(Arg264Gln) - missense -
./. - c.791G>A 791 r.(?) p.(Arg264Gln) - missense -
./. - c.791G>A 791 r.(?) p.(Arg264Gln) - missense -
./. - c.791G>A 791 r.(?) p.(Arg264Gln) - missense -
./. - c.791G>A 791 r.(?) p.(Arg264Gln) - missense -
./. - c.791G>A 791 r.(?) p.(Arg264Gln) - missense -
./. - c.791G>A 791 r.(?) p.(Arg264Gln) - missense -
./. - c.791G>A 791 r.(?) p.(Arg264Gln) - missense -
./. - c.791G>A 791 r.(?) p.(Arg264Gln) - missense -
./. - c.791G>A 791 r.(?) p.(Arg264Gln) - missense -
./. - c.791G>A 791 r.(?) p.(Arg264Gln) - missense -
./. - c.791G>A 791 r.(?) p.(Arg264Gln) - missense -
./. - c.791G>A 791 r.(?) p.(Arg264Gln) - missense -
./. - c.791G>A 791 r.(?) p.(Arg264Gln) - missense -
./. - c.791G>A 791 r.(?) p.(Arg264Gln) - missense -
./. - c.791G>A 791 r.(?) p.(Arg264Gln) - missense -
./. - c.1253G>A 1253 r.(?) p.(Arg418His) - missense -
./. - c.1393C>T 1393 r.(?) p.(=) - coding-synonymous -
./. - c.1393C>T 1393 r.(?) p.(=) - coding-synonymous -
./. - c.1393C>T 1393 r.(?) p.(=) - coding-synonymous -
./. - c.1393C>T 1393 r.(?) p.(=) - coding-synonymous -
./. - c.1393C>T 1393 r.(?) p.(=) - coding-synonymous -
./. - c.1393C>T 1393 r.(?) p.(=) - coding-synonymous -
./. - c.1393C>T 1393 r.(?) p.(=) - coding-synonymous -
./. - c.1407C>T 1407 r.(?) p.(=) - coding-synonymous -
./. - c.1407C>T 1407 r.(?) p.(=) - coding-synonymous -
./. - c.1407C>T 1407 r.(?) p.(=) - coding-synonymous -
./. - c.1407C>T 1407 r.(?) p.(=) - coding-synonymous -
./. - c.1407C>T 1407 r.(?) p.(=) - coding-synonymous -
./. - c.1407C>T 1407 r.(?) p.(=) - coding-synonymous -
./. - c.1407C>T 1407 r.(?) p.(=) - coding-synonymous -
./. - c.1591G>C 1591 r.(?) p.(Gly531Arg) - missense -
./. - c.1634+7C>G 1634 r.(=) p.(=) - splice 7
./. - c.1634+31C>T 1634 r.(=) p.(=) - intron 31
./. - c.1634+31C>T 1634 r.(=) p.(=) - intron 31
./. - c.1634+31C>T 1634 r.(=) p.(=) - intron 31
./. - c.1634+31C>T 1634 r.(=) p.(=) - intron 31
./. - c.1634+31C>T 1634 r.(=) p.(=) - intron 31
./. - c.1689+6T>C 1689 r.(=) p.(=) - splice 6
./. - c.1689+6T>C 1689 r.(=) p.(=) - splice 6
./. - c.1689+6T>C 1689 r.(=) p.(=) - splice 6
./. - c.1689+6T>C 1689 r.(=) p.(=) - splice 6
./. - c.1689+6T>C 1689 r.(=) p.(=) - splice 6
./. - c.1689+6T>C 1689 r.(=) p.(=) - splice 6
./. - c.1689+6T>C 1689 r.(=) p.(=) - splice 6
./. - c.1689+6T>C 1689 r.(=) p.(=) - splice 6
./. - c.1689+6T>C 1689 r.(=) p.(=) - splice 6
./. - c.1808C>T 1808 r.(?) p.(Thr603Met) - missense -
./. - c.1819C>T 1819 r.(?) p.(Leu607Phe) - missense -
./. - c.1819C>T 1819 r.(?) p.(Leu607Phe) - missense -
./. - c.1819C>T 1819 r.(?) p.(Leu607Phe) - missense -
./. - c.1819C>T 1819 r.(?) p.(Leu607Phe) - missense -
./. - c.1819C>T 1819 r.(?) p.(Leu607Phe) - missense -
./. - c.1819C>T 1819 r.(?) p.(Leu607Phe) - missense -
./. - c.1819C>T 1819 r.(?) p.(Leu607Phe) - missense -
./. - c.1819C>T 1819 r.(?) p.(Leu607Phe) - missense -
./. - c.1863G>A 1863 r.(?) p.(=) - coding-synonymous -
./. - c.1863G>A 1863 r.(?) p.(=) - coding-synonymous -
./. - c.1863G>A 1863 r.(?) p.(=) - coding-synonymous -
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