Transcript #00002999 (NM_001110556.1, FLNA gene)

Transcript name transcript variant 2
Gene name FLNA (filamin A, alpha)
Chromosome X
Transcript - NCBI ID NM_001110556.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001104026.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2013-10-29 14:41:43 +01:00 (CET)
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.663C>T 663 r.(?) p.(=) - coding-synonymous -
./. - c.869-41C>T 869 r.(=) p.(=) - intron 41
./. - c.869-41C>T 869 r.(=) p.(=) - intron 41
./. - c.869-41C>T 869 r.(=) p.(=) - intron 41
./. - c.869-41C>T 869 r.(=) p.(=) - intron 41
./. - c.869-41C>T 869 r.(=) p.(=) - intron 41
./. - c.869-28C>G 869 r.(=) p.(=) - intron 28
./. - c.869-28C>G 869 r.(=) p.(=) - intron 28
./. - c.869-28C>G 869 r.(=) p.(=) - intron 28
./. - c.869-28C>G 869 r.(=) p.(=) - intron 28
./. - c.869-28C>G 869 r.(=) p.(=) - intron 28
./. - c.869-28C>G 869 r.(=) p.(=) - intron 28
./. - c.869-28C>G 869 r.(=) p.(=) - intron 28
./. - c.869-28C>G 869 r.(=) p.(=) - intron 28
./. - c.869-23G>C 869 r.(=) p.(=) - intron 23
./. - c.869-23G>C 869 r.(=) p.(=) - intron 23
./. - c.1828+39C>T 1828 r.(=) p.(=) - intron 39
./. - c.1968C>T 1968 r.(?) p.(=) - coding-synonymous -
./. - c.3207+49G>A 3207 r.(=) p.(=) - intron 49
./. - c.4494C>T 4494 r.(?) p.(=) - coding-synonymous -
./. - c.4598+38A>G 4598 r.(=) p.(=) - intron 38
./. - c.4598+38A>G 4598 r.(=) p.(=) - intron 38
./. - c.4598+38A>G 4598 r.(=) p.(=) - intron 38
./. - c.4920G>A 4920 r.(?) p.(=) - coding-synonymous -
./. - c.4920G>A 4920 r.(?) p.(=) - coding-synonymous -
./. - c.4920G>A 4920 r.(?) p.(=) - coding-synonymous -
./. - c.4920G>A 4920 r.(?) p.(=) - coding-synonymous -
./. - c.5290G>A 5290 r.(?) p.(Ala1764Thr) - missense -
./. - c.5290G>A 5290 r.(?) p.(Ala1764Thr) - missense -
./. - c.5417-44C>T 5417 r.(=) p.(=) - intron 44
./. - c.5417-44C>T 5417 r.(=) p.(=) - intron 44
./. - c.5417-44C>T 5417 r.(=) p.(=) - intron 44
./. - c.5417-44C>T 5417 r.(=) p.(=) - intron 44
./. - c.5417-44C>T 5417 r.(=) p.(=) - intron 44
./. - c.5814C>T 5814 r.(?) p.(=) - coding-synonymous -
./. - c.5850T>C 5850 r.(?) p.(=) - coding-synonymous -
./. - c.5850T>C 5850 r.(?) p.(=) - coding-synonymous -
./. - c.5850T>C 5850 r.(?) p.(=) - coding-synonymous -
./. - c.5850T>C 5850 r.(?) p.(=) - coding-synonymous -
./. - c.5850T>C 5850 r.(?) p.(=) - coding-synonymous -
./. - c.5850T>C 5850 r.(?) p.(=) - coding-synonymous -
./. - c.6022+45G>A 6022 r.(=) p.(=) - intron 45
./. - c.6022+45G>A 6022 r.(=) p.(=) - intron 45
./. - c.6022+45G>A 6022 r.(=) p.(=) - intron 45
./. - c.6022+45G>A 6022 r.(=) p.(=) - intron 45
./. - c.6023-10C>G 6023 r.(=) p.(=) - intron 10
./. - c.6642G>C 6642 r.(?) p.(=) - coding-synonymous -
./. - c.7024-39T>C 7024 r.(=) p.(=) - intron 39
./. - c.7024-39T>C 7024 r.(=) p.(=) - intron 39
./. - c.7024-39T>C 7024 r.(=) p.(=) - intron 39
./. - c.7024-39T>C 7024 r.(=) p.(=) - intron 39
./. - c.7024-39T>C 7024 r.(=) p.(=) - intron 39
./. - c.7024-39T>C 7024 r.(=) p.(=) - intron 39
./. - c.7024-39T>C 7024 r.(=) p.(=) - intron 39
./. - c.7024-39T>C 7024 r.(=) p.(=) - intron 39
./. - c.7024-39T>C 7024 r.(=) p.(=) - intron 39
./. - c.7024-39T>C 7024 r.(=) p.(=) - intron 39
./. - c.7024-39T>C 7024 r.(=) p.(=) - intron 39
./. - c.7224C>T 7224 r.(?) p.(=) - coding-synonymous -
./. - c.7434G>A 7434 r.(?) p.(=) - coding-synonymous -
./. - c.7552+36C>T 7552 r.(=) p.(=) - intron 36
./. - c.7756+11C>T 7756 r.(=) p.(=) - intron 11
./. - c.7756+11C>T 7756 r.(=) p.(=) - intron 11
./. - c.7756+11C>T 7756 r.(=) p.(=) - intron 11
./. - c.7756+11C>T 7756 r.(=) p.(=) - intron 11
./. - c.7756+11C>T 7756 r.(=) p.(=) - intron 11
./. - c.7756+11C>T 7756 r.(=) p.(=) - intron 11
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