Transcript #00006688 (NM_001256071.1, RNF213 gene)

Transcript name transcript variant 3
Gene name RNF213 (ring finger protein 213)
Chromosome 17
Transcript - NCBI ID NM_001256071.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001243000.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2013-10-30 12:06:09 +01:00 (CET)
Date last edited N/A


Variants

375 entries on 4 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.98-44_98-43insACTT 98 r.(=) p.(=) - intron 43
./. - c.126G>A 126 r.(?) p.(=) - coding-synonymous -
./. - c.222C>T 222 r.(?) p.(=) - coding-synonymous -
./. - c.261+27C>T 261 r.(=) p.(=) - intron 27
./. - c.378G>A 378 r.(?) p.(=) - coding-synonymous -
./. - c.378G>A 378 r.(?) p.(=) - coding-synonymous -
./. - c.378G>A 378 r.(?) p.(=) - coding-synonymous -
./. - c.378G>A 378 r.(?) p.(=) - coding-synonymous -
./. - c.378G>A 378 r.(?) p.(=) - coding-synonymous -
./. - c.378G>A 378 r.(?) p.(=) - coding-synonymous -
./. - c.378G>A 378 r.(?) p.(=) - coding-synonymous -
./. - c.378G>A 378 r.(?) p.(=) - coding-synonymous -
./. - c.378G>A 378 r.(?) p.(=) - coding-synonymous -
./. - c.378G>A 378 r.(?) p.(=) - coding-synonymous -
./. - c.447G>A 447 r.(?) p.(=) - coding-synonymous -
./. - c.453A>G 453 r.(?) p.(=) - coding-synonymous -
./. - c.453A>G 453 r.(?) p.(=) - coding-synonymous -
./. - c.453A>G 453 r.(?) p.(=) - coding-synonymous -
./. - c.453A>G 453 r.(?) p.(=) - coding-synonymous -
./. - c.453A>G 453 r.(?) p.(=) - coding-synonymous -
./. - c.453A>G 453 r.(?) p.(=) - coding-synonymous -
./. - c.453A>G 453 r.(?) p.(=) - coding-synonymous -
./. - c.453A>G 453 r.(?) p.(=) - coding-synonymous -
./. - c.453A>G 453 r.(?) p.(=) - coding-synonymous -
./. - c.453A>G 453 r.(?) p.(=) - coding-synonymous -
./. - c.453A>G 453 r.(?) p.(=) - coding-synonymous -
./. - c.453A>G 453 r.(?) p.(=) - coding-synonymous -
./. - c.453A>G 453 r.(?) p.(=) - coding-synonymous -
./. - c.453A>G 453 r.(?) p.(=) - coding-synonymous -
./. - c.809T>C 809 r.(?) p.(Met270Thr) - missense-near-splice -
./. - c.809T>C 809 r.(?) p.(Met270Thr) - missense-near-splice -
./. - c.809T>C 809 r.(?) p.(Met270Thr) - missense-near-splice -
./. - c.809T>C 809 r.(?) p.(Met270Thr) - missense-near-splice -
./. - c.809T>C 809 r.(?) p.(Met270Thr) - missense-near-splice -
./. - c.809T>C 809 r.(?) p.(Met270Thr) - missense-near-splice -
./. - c.809T>C 809 r.(?) p.(Met270Thr) - missense-near-splice -
./. - c.809T>C 809 r.(?) p.(Met270Thr) - missense-near-splice -
./. - c.809T>C 809 r.(?) p.(Met270Thr) - missense-near-splice -
./. - c.809T>C 809 r.(?) p.(Met270Thr) - missense-near-splice -
./. - c.809T>C 809 r.(?) p.(Met270Thr) - missense-near-splice -
./. - c.934-29C>G 934 r.(=) p.(=) - intron 29
./. - c.934-29C>G 934 r.(=) p.(=) - intron 29
./. - c.934-29C>G 934 r.(=) p.(=) - intron 29
./. - c.934-29C>G 934 r.(=) p.(=) - intron 29
./. - c.934-29C>G 934 r.(=) p.(=) - intron 29
./. - c.934-29C>G 934 r.(=) p.(=) - intron 29
./. - c.934-29C>G 934 r.(=) p.(=) - intron 29
./. - c.934-29C>G 934 r.(=) p.(=) - intron 29
./. - c.934-29C>G 934 r.(=) p.(=) - intron 29
./. - c.934-29C>G 934 r.(=) p.(=) - intron 29
./. - c.934-29C>G 934 r.(=) p.(=) - intron 29
./. - c.962T>C 962 r.(?) p.(Met321Thr) - missense -
./. - c.962T>C 962 r.(?) p.(Met321Thr) - missense -
./. - c.962T>C 962 r.(?) p.(Met321Thr) - missense -
./. - c.962T>C 962 r.(?) p.(Met321Thr) - missense -
./. - c.962T>C 962 r.(?) p.(Met321Thr) - missense -
./. - c.962T>C 962 r.(?) p.(Met321Thr) - missense -
./. - c.962T>C 962 r.(?) p.(Met321Thr) - missense -
./. - c.962T>C 962 r.(?) p.(Met321Thr) - missense -
./. - c.962T>C 962 r.(?) p.(Met321Thr) - missense -
./. - c.962T>C 962 r.(?) p.(Met321Thr) - missense -
./. - c.962T>C 962 r.(?) p.(Met321Thr) - missense -
./. - c.962T>C 962 r.(?) p.(Met321Thr) - missense -
./. - c.990G>A 990 r.(?) p.(=) - coding-synonymous -
./. - c.990G>A 990 r.(?) p.(=) - coding-synonymous -
./. - c.990G>A 990 r.(?) p.(=) - coding-synonymous -
./. - c.990G>A 990 r.(?) p.(=) - coding-synonymous -
./. - c.990G>A 990 r.(?) p.(=) - coding-synonymous -
./. - c.990G>A 990 r.(?) p.(=) - coding-synonymous -
./. - c.990G>A 990 r.(?) p.(=) - coding-synonymous -
./. - c.990G>A 990 r.(?) p.(=) - coding-synonymous -
./. - c.990G>A 990 r.(?) p.(=) - coding-synonymous -
./. - c.990G>A 990 r.(?) p.(=) - coding-synonymous -
./. - c.990G>A 990 r.(?) p.(=) - coding-synonymous -
./. - c.990G>A 990 r.(?) p.(=) - coding-synonymous -
./. - c.1271+19T>G 1271 r.(=) p.(=) - intron 19
./. - c.1271+19T>G 1271 r.(=) p.(=) - intron 19
./. - c.1271+19T>G 1271 r.(=) p.(=) - intron 19
./. - c.1271+19T>G 1271 r.(=) p.(=) - intron 19
./. - c.1271+19T>G 1271 r.(=) p.(=) - intron 19
./. - c.1271+19T>G 1271 r.(=) p.(=) - intron 19
./. - c.1271+19T>G 1271 r.(=) p.(=) - intron 19
./. - c.1407G>T 1407 r.(?) p.(Gln469His) - missense -
./. - c.1471+41T>C 1471 r.(=) p.(=) - intron 41
./. - c.1471+41T>C 1471 r.(=) p.(=) - intron 41
./. - c.1471+41T>C 1471 r.(=) p.(=) - intron 41
./. - c.1471+41T>C 1471 r.(=) p.(=) - intron 41
./. - c.1471+41T>C 1471 r.(=) p.(=) - intron 41
./. - c.1471+41T>C 1471 r.(=) p.(=) - intron 41
./. - c.1471+41T>C 1471 r.(=) p.(=) - intron 41
./. - c.1471+41T>C 1471 r.(=) p.(=) - intron 41
./. - c.1471+41T>C 1471 r.(=) p.(=) - intron 41
./. - c.1471+41T>C 1471 r.(=) p.(=) - intron 41
./. - c.1471+41T>C 1471 r.(=) p.(=) - intron 41
./. - c.1471+41T>C 1471 r.(=) p.(=) - intron 41
./. - c.1471+41T>C 1471 r.(=) p.(=) - intron 41
./. - c.1471+41T>C 1471 r.(=) p.(=) - intron 41
./. - c.1471+41T>C 1471 r.(=) p.(=) - intron 41
./. - c.1471+41T>C 1471 r.(=) p.(=) - intron 41
./. - c.1471+41T>C 1471 r.(=) p.(=) - intron 41
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