Transcript #00020104 (NM_001170416.1, TJP2 gene)

Transcript name Manually created transcript.
Gene name TJP2 (tight junction protein 2)
Chromosome 9
Transcript - NCBI ID NM_001170416.1
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

175 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.207+35T>C 207 r.(=) p.(=) - intron 35
./. - c.207+35T>C 207 r.(=) p.(=) - intron 35
./. - c.207+35T>C 207 r.(=) p.(=) - intron 35
./. - c.332+19T>C 332 r.(=) p.(=) - intron 19
./. - c.332+19T>C 332 r.(=) p.(=) - intron 19
./. - c.332+19T>C 332 r.(=) p.(=) - intron 19
./. - c.332+19T>C 332 r.(=) p.(=) - intron 19
./. - c.332+19T>C 332 r.(=) p.(=) - intron 19
./. - c.332+19T>C 332 r.(=) p.(=) - intron 19
./. - c.332+19T>C 332 r.(=) p.(=) - intron 19
./. - c.332+19T>C 332 r.(=) p.(=) - intron 19
./. - c.332+19T>C 332 r.(=) p.(=) - intron 19
./. - c.332+19T>C 332 r.(=) p.(=) - intron 19
./. - c.332+19T>C 332 r.(=) p.(=) - intron 19
./. - c.332+19T>C 332 r.(=) p.(=) - intron 19
./. - c.332+19T>C 332 r.(=) p.(=) - intron 19
./. - c.332+19T>C 332 r.(=) p.(=) - intron 19
./. - c.332+19T>C 332 r.(=) p.(=) - intron 19
./. - c.332+19T>C 332 r.(=) p.(=) - intron 19
./. - c.332+19T>C 332 r.(=) p.(=) - intron 19
./. - c.332+19T>C 332 r.(=) p.(=) - intron 19
./. - c.332+19T>C 332 r.(=) p.(=) - intron 19
./. - c.332+19T>C 332 r.(=) p.(=) - intron 19
./. - c.332+19T>C 332 r.(=) p.(=) - intron 19
./. - c.332+19T>C 332 r.(=) p.(=) - intron 19
./. - c.332+19T>C 332 r.(=) p.(=) - intron 19
./. - c.332+19T>C 332 r.(=) p.(=) - intron 19
./. - c.332+19T>C 332 r.(=) p.(=) - intron 19
./. - c.332+19T>C 332 r.(=) p.(=) - intron 19
./. - c.332+19T>C 332 r.(=) p.(=) - intron 19
./. - c.332+19T>C 332 r.(=) p.(=) - intron 19
./. - c.332+19T>C 332 r.(=) p.(=) - intron 19
./. - c.332+19T>C 332 r.(=) p.(=) - intron 19
./. - c.332+19T>C 332 r.(=) p.(=) - intron 19
./. - c.390G>A 390 r.(?) p.(=) - coding-synonymous -
./. - c.435+12G>T 435 r.(=) p.(=) - intron 12
./. - c.436-28G>A 436 r.(=) p.(=) - intron 28
./. - c.436-28G>A 436 r.(=) p.(=) - intron 28
./. - c.436-28G>A 436 r.(=) p.(=) - intron 28
./. - c.436-28G>A 436 r.(=) p.(=) - intron 28
./. - c.436-28G>A 436 r.(=) p.(=) - intron 28
./. - c.436-28G>A 436 r.(=) p.(=) - intron 28
./. - c.436-28G>A 436 r.(=) p.(=) - intron 28
./. - c.436-28G>A 436 r.(=) p.(=) - intron 28
./. - c.468C>T 468 r.(?) p.(=) - coding-synonymous -
./. - c.475C>A 475 r.(?) p.(Gln159Lys) - missense -
./. - c.475C>A 475 r.(?) p.(Gln159Lys) - missense -
./. - c.475C>A 475 r.(?) p.(Gln159Lys) - missense -
./. - c.475C>A 475 r.(?) p.(Gln159Lys) - missense -
./. - c.475C>A 475 r.(?) p.(Gln159Lys) - missense -
./. - c.475C>A 475 r.(?) p.(Gln159Lys) - missense -
./. - c.475C>A 475 r.(?) p.(Gln159Lys) - missense -
./. - c.475C>A 475 r.(?) p.(Gln159Lys) - missense -
./. - c.1045+39A>G 1045 r.(=) p.(=) - intron 39
./. - c.1045+39A>G 1045 r.(=) p.(=) - intron 39
./. - c.1184C>T 1184 r.(?) p.(Thr395Met) - missense -
./. - c.1230A>G 1230 r.(?) p.(=) - coding-synonymous -
./. - c.1230A>G 1230 r.(?) p.(=) - coding-synonymous -
./. - c.1230A>G 1230 r.(?) p.(=) - coding-synonymous -
./. - c.1230A>G 1230 r.(?) p.(=) - coding-synonymous -
./. - c.1230A>G 1230 r.(?) p.(=) - coding-synonymous -
./. - c.1443C>T 1443 r.(?) p.(=) - coding-synonymous -
./. - c.1443C>T 1443 r.(?) p.(=) - coding-synonymous -
./. - c.1539C>A 1539 r.(?) p.(Asp513Glu) - missense -
./. - c.1539C>A 1539 r.(?) p.(Asp513Glu) - missense -
./. - c.1539C>A 1539 r.(?) p.(Asp513Glu) - missense -
./. - c.1539C>A 1539 r.(?) p.(Asp513Glu) - missense -
./. - c.1539C>A 1539 r.(?) p.(Asp513Glu) - missense -
./. - c.1539C>A 1539 r.(?) p.(Asp513Glu) - missense -
./. - c.1539C>A 1539 r.(?) p.(Asp513Glu) - missense -
./. - c.1539C>A 1539 r.(?) p.(Asp513Glu) - missense -
./. - c.1539C>A 1539 r.(?) p.(Asp513Glu) - missense -
./. - c.1539C>A 1539 r.(?) p.(Asp513Glu) - missense -
./. - c.1539C>A 1539 r.(?) p.(Asp513Glu) - missense -
./. - c.1539C>A 1539 r.(?) p.(Asp513Glu) - missense -
./. - c.1539C>A 1539 r.(?) p.(Asp513Glu) - missense -
./. - c.1539C>A 1539 r.(?) p.(Asp513Glu) - missense -
./. - c.1539C>A 1539 r.(?) p.(Asp513Glu) - missense -
./. - c.1539C>A 1539 r.(?) p.(Asp513Glu) - missense -
./. - c.1539C>A 1539 r.(?) p.(Asp513Glu) - missense -
./. - c.1539C>A 1539 r.(?) p.(Asp513Glu) - missense -
./. - c.1539C>A 1539 r.(?) p.(Asp513Glu) - missense -
./. - c.1539C>A 1539 r.(?) p.(Asp513Glu) - missense -
./. - c.1539C>A 1539 r.(?) p.(Asp513Glu) - missense -
./. - c.1539C>A 1539 r.(?) p.(Asp513Glu) - missense -
./. - c.1539C>A 1539 r.(?) p.(Asp513Glu) - missense -
./. - c.1539C>A 1539 r.(?) p.(Asp513Glu) - missense -
./. - c.1539C>A 1539 r.(?) p.(Asp513Glu) - missense -
./. - c.1539C>A 1539 r.(?) p.(Asp513Glu) - missense -
./. - c.1539C>A 1539 r.(?) p.(Asp513Glu) - missense -
./. - c.1539C>A 1539 r.(?) p.(Asp513Glu) - missense -
./. - c.1765-20C>G 1765 r.(=) p.(=) - intron 20
./. - c.1765-20C>G 1765 r.(=) p.(=) - intron 20
./. - c.1765-20C>G 1765 r.(=) p.(=) - intron 20
./. - c.1765-20C>G 1765 r.(=) p.(=) - intron 20
./. - c.2097G>A 2097 r.(?) p.(Met699Ile) - missense -
./. - c.2097G>A 2097 r.(?) p.(Met699Ile) - missense -
./. - c.2097G>A 2097 r.(?) p.(Met699Ile) - missense -
./. - c.2133G>A 2133 r.(?) p.(=) - coding-synonymous -
./. - c.2133G>A 2133 r.(?) p.(=) - coding-synonymous -
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