Transcript #00004549 (NM_001123066.3, MAPT gene)

Transcript name transcript variant 6
Gene name MAPT (microtubule-associated protein tau)
Chromosome 17
Transcript - NCBI ID NM_001123066.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_001116538.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2013-10-29 17:20:48 +01:00 (CET)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

Position     

RNA change     

Protein     

PolyPhen prediction     

GVS function     

Splice distance     
./. - c.-13A>G -13 r.(=) p.(=) - utr-5 -
./. - c.-13A>G -13 r.(=) p.(=) - utr-5 -
./. - c.-13A>G -13 r.(=) p.(=) - utr-5 -
./. - c.-13A>G -13 r.(=) p.(=) - utr-5 -
./. - c.-13A>G -13 r.(=) p.(=) - utr-5 -
./. - c.-13A>G -13 r.(=) p.(=) - utr-5 -
./. - c.-13A>G -13 r.(=) p.(=) - utr-5 -
./. - c.-13A>G -13 r.(=) p.(=) - utr-5 -
./. - c.220+18C>T 220 r.(=) p.(=) - intron 18
./. - c.220+18C>T 220 r.(=) p.(=) - intron 18
./. - c.220+18C>T 220 r.(=) p.(=) - intron 18
./. - c.307+9A>G 307 r.(=) p.(=) - intron 9
./. - c.307+9A>G 307 r.(=) p.(=) - intron 9
./. - c.307+9A>G 307 r.(=) p.(=) - intron 9
./. - c.307+9A>G 307 r.(=) p.(=) - intron 9
./. - c.605C>T 605 r.(?) p.(Pro202Leu) - missense -
./. - c.605C>T 605 r.(?) p.(Pro202Leu) - missense -
./. - c.605C>T 605 r.(?) p.(Pro202Leu) - missense -
./. - c.853G>A 853 r.(?) p.(Asp285Asn) - missense -
./. - c.853G>A 853 r.(?) p.(Asp285Asn) - missense -
./. - c.853G>A 853 r.(?) p.(Asp285Asn) - missense -
./. - c.853G>A 853 r.(?) p.(Asp285Asn) - missense -
./. - c.853G>A 853 r.(?) p.(Asp285Asn) - missense -
./. - c.853G>A 853 r.(?) p.(Asp285Asn) - missense -
./. - c.853G>A 853 r.(?) p.(Asp285Asn) - missense -
./. - c.853G>A 853 r.(?) p.(Asp285Asn) - missense -
./. - c.853G>A 853 r.(?) p.(Asp285Asn) - missense -
./. - c.855C>T 855 r.(?) p.(=) - coding-synonymous -
./. - c.855C>T 855 r.(?) p.(=) - coding-synonymous -
./. - c.855C>T 855 r.(?) p.(=) - coding-synonymous -
./. - c.855C>T 855 r.(?) p.(=) - coding-synonymous -
./. - c.866T>C 866 r.(?) p.(Val289Ala) - missense -
./. - c.866T>C 866 r.(?) p.(Val289Ala) - missense -
./. - c.866T>C 866 r.(?) p.(Val289Ala) - missense -
./. - c.866T>C 866 r.(?) p.(Val289Ala) - missense -
./. - c.866T>C 866 r.(?) p.(Val289Ala) - missense -
./. - c.866T>C 866 r.(?) p.(Val289Ala) - missense -
./. - c.866T>C 866 r.(?) p.(Val289Ala) - missense -
./. - c.953C>T 953 r.(?) p.(Ser318Leu) - missense -
./. - c.953C>T 953 r.(?) p.(Ser318Leu) - missense -
./. - c.953C>T 953 r.(?) p.(Ser318Leu) - missense -
./. - c.953C>T 953 r.(?) p.(Ser318Leu) - missense -
./. - c.1108C>T 1108 r.(?) p.(Arg370Trp) - missense -
./. - c.1108C>T 1108 r.(?) p.(Arg370Trp) - missense -
./. - c.1108C>T 1108 r.(?) p.(Arg370Trp) - missense -
./. - c.1108C>T 1108 r.(?) p.(Arg370Trp) - missense -
./. - c.1108C>T 1108 r.(?) p.(Arg370Trp) - missense -
./. - c.1108C>T 1108 r.(?) p.(Arg370Trp) - missense -
./. - c.1108C>T 1108 r.(?) p.(Arg370Trp) - missense -
./. - c.1108C>T 1108 r.(?) p.(Arg370Trp) - missense -
./. - c.1321T>C 1321 r.(?) p.(Tyr441His) - missense -
./. - c.1321T>C 1321 r.(?) p.(Tyr441His) - missense -
./. - c.1321T>C 1321 r.(?) p.(Tyr441His) - missense -
./. - c.1321T>C 1321 r.(?) p.(Tyr441His) - missense -
./. - c.1321T>C 1321 r.(?) p.(Tyr441His) - missense -
./. - c.1321T>C 1321 r.(?) p.(Tyr441His) - missense -
./. - c.1321T>C 1321 r.(?) p.(Tyr441His) - missense -
./. - c.1321T>C 1321 r.(?) p.(Tyr441His) - missense -
./. - c.1321T>C 1321 r.(?) p.(Tyr441His) - missense -
./. - c.1321T>C 1321 r.(?) p.(Tyr441His) - missense -
./. - c.1321T>C 1321 r.(?) p.(Tyr441His) - missense -
./. - c.1321T>C 1321 r.(?) p.(Tyr441His) - missense -
./. - c.1321T>C 1321 r.(?) p.(Tyr441His) - missense -
./. - c.1321T>C 1321 r.(?) p.(Tyr441His) - missense -
./. - c.1321T>C 1321 r.(?) p.(Tyr441His) - missense -
./. - c.1321T>C 1321 r.(?) p.(Tyr441His) - missense -
./. - c.1321T>C 1321 r.(?) p.(Tyr441His) - missense -
./. - c.1321T>C 1321 r.(?) p.(Tyr441His) - missense -
./. - c.1339T>C 1339 r.(?) p.(Ser447Pro) - missense -
./. - c.1339T>C 1339 r.(?) p.(Ser447Pro) - missense -
./. - c.1479G>A 1479 r.(?) p.(=) - coding-synonymous -
./. - c.1479G>A 1479 r.(?) p.(=) - coding-synonymous -
./. - c.1479G>A 1479 r.(?) p.(=) - coding-synonymous -
./. - c.1479G>A 1479 r.(?) p.(=) - coding-synonymous -
./. - c.1479G>A 1479 r.(?) p.(=) - coding-synonymous -
./. - c.1483G>A 1483 r.(?) p.(Ala495Thr) - missense -
./. - c.1512T>C 1512 r.(?) p.(=) - coding-synonymous -
./. - c.1512T>C 1512 r.(?) p.(=) - coding-synonymous -
./. - c.1512T>C 1512 r.(?) p.(=) - coding-synonymous -
./. - c.1512T>C 1512 r.(?) p.(=) - coding-synonymous -
./. - c.1512T>C 1512 r.(?) p.(=) - coding-synonymous -
./. - c.1512T>C 1512 r.(?) p.(=) - coding-synonymous -
./. - c.1512T>C 1512 r.(?) p.(=) - coding-synonymous -
./. - c.1512T>C 1512 r.(?) p.(=) - coding-synonymous -
./. - c.1512T>C 1512 r.(?) p.(=) - coding-synonymous -
./. - c.1512T>C 1512 r.(?) p.(=) - coding-synonymous -
./. - c.1534C>T 1534 r.(?) p.(Pro512Ser) - missense -
./. - c.1562-31T>C 1562 r.(=) p.(=) - intron 31
./. - c.1562-31T>C 1562 r.(=) p.(=) - intron 31
./. - c.1562-26G>A 1562 r.(=) p.(=) - intron 26
./. - c.1562-26G>A 1562 r.(=) p.(=) - intron 26
./. - c.1562-26G>A 1562 r.(=) p.(=) - intron 26
./. - c.1562-26G>A 1562 r.(=) p.(=) - intron 26
./. - c.1562-26G>A 1562 r.(=) p.(=) - intron 26
./. - c.1562-26G>A 1562 r.(=) p.(=) - intron 26
./. - c.1562-26G>A 1562 r.(=) p.(=) - intron 26
./. - c.1562-26G>A 1562 r.(=) p.(=) - intron 26
./. - c.1631G>A 1631 r.(?) p.(Arg544His) - missense -
./. - c.1686A>G 1686 r.(?) p.(=) - coding-synonymous -
./. - c.1686A>G 1686 r.(?) p.(=) - coding-synonymous -
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