Transcript #00006191

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 -


Variants

380 entries on 4 pages. Showing entries 1 - 100.
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Affects function     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/? c.-19del r.(=) p.(=)
?/? c.-19dup r.(=) p.(=)
?/? c.64_65insTCG r.(?) p.(Val21dup)
?/? c.234C>A r.(=) p.(=)
?/? c.240G>C r.(=) p.(=)
?/? c.373+10G>T r.(=) p.(=)
?/? c.373+39G>A r.(=) p.(=)
?/? c.373+41A>T r.(=) p.(=)
?/? c.374-52C>T r.(=) p.(=)
?/? c.374-51G>A r.(=) p.(=)
?/? c.374-43C>A r.(=) p.(=)
?/? c.374-40C>T r.(=) p.(=)
?/? c.374-34C>T r.(=) p.(=)
?/? c.374-19G>A r.(=) p.(=)
?/? c.387C>T r.(=) p.(=)
?/? c.543G>C r.(=) p.(=)
?/? c.597C>T r.(=) p.(=)
?/? c.622+18C>A r.(=) p.(=)
?/? c.622+23G>A r.(=) p.(=)
?/? c.623-49T>C r.(=) p.(=)
?/? c.623-5C>T r.spl? p.?
?/? c.651C>T r.(=) p.(=)
?/? c.663C>T r.(=) p.(=)
?/? c.675G>A r.(=) p.(=)
?/? c.720+8C>T r.(=) p.(=)
?/? c.720+12C>T r.(=) p.(=)
?/? c.720+42C>T r.(=) p.(=)
?/? c.720+44G>T r.(=) p.(=)
?/? c.721-46G>T r.(=) p.(=)
?/? c.721-11G>A r.(=) p.(=)
?/? c.732C>T r.(=) p.(=)
?/? c.753C>T r.(=) p.(=)
?/? c.861C>T r.(=) p.(=)
?/? c.868+33G>A r.(=) p.(=)
?/? c.869-47T>C r.(=) p.(=)
?/? c.869-46G>A r.(=) p.(=)
?/? c.869-41C>T r.(=) p.(=)
?/? c.869-28C>G r.(=) p.(=)
?/? c.869-26G>A r.(=) p.(=)
?/? c.869-23G>C r.(=) p.(=)
?/? c.869-7C>T r.(=) p.(=)
?/? c.882A>G r.(=) p.(=)
?/? c.901C>T r.(?) p.(Arg301Trp)
?/? c.902G>T r.(?) p.(Arg301Leu)
?/? c.942A>G r.(=) p.(=)
?/? c.957C>T r.(=) p.(=)
?/? c.968C>T r.(?) p.(Pro323Leu)
?/? c.987+12T>A r.(=) p.(=)
?/? c.988-14C>T r.(=) p.(=)
?/? c.1019G>T r.(?) p.(Arg340Leu)
?/? c.1029C>T r.(=) p.(=)
?/? c.1044C>T r.(=) p.(=)
?/? c.1045G>A r.(?) p.(Glu349Lys)
?/? c.1054G>A r.(?) p.(Gly352Arg)
?/? c.1066-22C>T r.(=) p.(=)
?/? c.1066-19C>T r.(=) p.(=)
?/? c.1093A>G r.(?) p.(Ile365Val)
?/? c.1095C>T r.(=) p.(=)
?/? c.1167C>T r.(=) p.(=)
?/? c.1176G>A r.(=) p.(=)
?/? c.1180A>G r.(?) p.(Ser394Gly)
?/? c.1191C>T r.(=) p.(=)
?/? c.1229-8C>T r.(=) p.(=)
?/? c.1239G>A r.(=) p.(=)
?/? c.1249G>A r.(?) p.(Glu417Lys)
?/? c.1266C>T r.(=) p.(=)
?/? c.1285A>T r.(?) p.(Thr429Ser)
?/? c.1286C>T r.(?) p.(Thr429Met)
?/? c.1376C>T r.(?) p.(Thr459Met)
?/? c.1383C>T r.(=) p.(=)
?/? c.1399C>T r.(?) p.(Arg467Cys)
?/? c.1429+8C>T r.(=) p.(=)
?/? c.1429+39A>T r.(=) p.(=)
?/? c.1430-44G>A r.(=) p.(=)
?/? c.1450C>T r.(?) p.(Arg484Trp)
?/? c.1567+35C>T r.(=) p.(=)
?/? c.1567+45_1568-44insC r.spl? p.?
?/? c.1568-36T>C r.(=) p.(=)
?/? c.1568-32G>A r.(=) p.(=)
?/? c.1579C>T r.(?) p.(Arg527Cys)
?/? c.1653C>T r.(=) p.(=)
?/? c.1691+7C>A r.(=) p.(=)
?/? c.1691+46_1691+50del r.(=) p.(=)
?/? c.1692-40_1692-38del r.(=) p.(=)
?/? c.1692-21G>A r.(=) p.(=)
?/? c.1710G>A r.(=) p.(=)
?/? c.1716C>T r.(=) p.(=)
?/? c.1756C>T r.(=) p.(=)
?/? c.1761G>A r.(=) p.(=)
?/? c.1767C>T r.(=) p.(=)
?/? c.1794G>A r.(=) p.(=)
?/? c.1807G>A r.(?) p.(Gly603Arg)
?/? c.1812C>T r.(=) p.(=)
?/? c.1828+3A>G r.spl? p.?
?/? c.1828+31G>C r.(=) p.(=)
?/? c.1829-13T>C r.(=) p.(=)
?/? c.1875C>T r.(=) p.(=)
?/? c.1881C>T r.(=) p.(=)
?/? c.1900C>T r.(?) p.(Arg634Cys)
?/? c.1933G>A r.(?) p.(Val645Ile)
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