Transcript #00003569

Transcript name cyclic nucleotide gated channel alpha 2
Gene name CNGA2 (cyclic nucleotide gated channel alpha 2)
Chromosome X
Transcript - NCBI ID NM_005140.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_005131.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

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

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/? c.6C>T r.(=) p.(=)
?/? c.10A>G r.(?) p.(Lys4Glu)
?/? c.44A>C r.(?) p.(Asn15Thr)
?/? c.61C>A r.(?) p.(Pro21Thr)
?/? c.106A>G r.(?) p.(Ser36Gly)
?/? c.111-51G>A r.(=) p.(=)
?/? c.111-19T>C r.(=) p.(=)
?/? c.111-3C>T r.spl? p.?
?/? c.129C>T r.(=) p.(=)
?/? c.138C>T r.(=) p.(=)
?/? c.145G>A r.(?) p.(Glu49Lys)
?/? c.199C>T r.(?) p.(Arg67Cys)
?/? c.204-33C>T r.(=) p.(=)
?/? c.204-30T>C r.(=) p.(=)
?/? c.211C>T r.(?) p.(Arg71Cys)
?/? c.212G>A r.(?) p.(Arg71His)
?/? c.230G>C r.(?) p.(Arg77Thr)
?/? c.254G>A r.(?) p.(Arg85Gln)
?/? c.285C>T r.(=) p.(=)
?/? c.286G>A r.(?) p.(Glu96Lys)
?/? c.289C>T r.(?) p.(Arg97Cys)
?/? c.338G>T r.(?) p.(Gly113Val)
?/? c.352G>C r.(?) p.(Asp118His)
?/? c.358G>A r.(?) p.(Glu120Lys)
?/? c.360G>A r.(=) p.(=)
?/? c.374+28A>G r.(=) p.(=)
?/? c.375-44T>A r.(=) p.(=)
?/? c.379A>G r.(?) p.(Lys127Glu)
?/? c.394G>T r.(?) p.(Val132Phe)
?/? c.402C>T r.(=) p.(=)
?/? c.416G>T r.(?) p.(Trp139Leu)
?/? c.419A>G r.(?) p.(Tyr140Cys)
?/? c.451G>A r.(?) p.(Val151Ile)
?/? c.479C>G r.(?) p.(Ala160Gly)
?/? c.482+1G>A r.spl? p.?
?/? c.482+18C>G r.(=) p.(=)
?/? c.483-32_483-31insG r.(=) p.(=)
?/? c.483-22G>A r.(=) p.(=)
?/? c.483-9C>T r.(=) p.(=)
?/? c.483-5C>T r.spl? p.?
?/? c.564G>A r.(=) p.(=)
?/? c.578G>A r.(?) p.(Arg193Gln)
?/? c.582G>A r.(=) p.(=)
?/? c.584G>A r.(?) p.(Arg195His)
?/? c.589+35G>C r.(=) p.(=)
?/? c.590-34G>A r.(=) p.(=)
?/? c.590-22T>C r.(=) p.(=)
?/? c.597G>A r.(=) p.(=)
?/? c.606G>A r.(=) p.(=)
?/? c.616A>G r.(?) p.(Lys206Glu)
?/? c.621T>G r.(?) p.(Asp207Glu)
?/? c.636A>G r.(=) p.(=)
?/? c.796C>T r.(?) p.(Arg266Cys)
?/? c.821G>A r.(?) p.(Arg274His)
?/? c.827G>A r.(?) p.(Ser276Asn)
?/? c.840C>T r.(=) p.(=)
?/? c.842A>C r.(?) p.(Tyr281Ser)
?/? c.852C>T r.(=) p.(=)
?/? c.881A>G r.(?) p.(Tyr294Cys)
?/? c.885C>T r.(=) p.(=)
?/? c.891C>T r.(=) p.(=)
?/? c.899T>A r.(?) p.(Ile300Lys)
?/? c.953G>A r.(?) p.(Gly318Asp)
?/? c.1013T>C r.(?) p.(Ile338Thr)
?/? c.1017G>A r.(=) p.(=)
?/? c.1081G>A r.(?) p.(Val361Ile)
?/? c.1101C>T r.(=) p.(=)
?/? c.1124T>C r.(?) p.(Ile375Thr)
?/? c.1145G>A r.(?) p.(Arg382Gln)
?/? c.1168G>A r.(?) p.(Asp390Asn)
?/? c.1180C>T r.(?) p.(His394Tyr)
?/? c.1190A>T r.(?) p.(Gln397Leu)
?/? c.1195C>T r.(?) p.(Arg399*)
?/? c.1196G>A r.(?) p.(Arg399Gln)
?/? c.1329T>C r.(=) p.(=)
?/? c.1331T>C r.(?) p.(Val444Ala)
?/? c.1361T>C r.(?) p.(Ile454Thr)
?/? c.1393G>C r.(?) p.(Glu465Gln)
?/? c.1448G>A r.(?) p.(Arg483His)
?/? c.1455G>C r.(=) p.(=)
?/? c.1458C>T r.(=) p.(=)
?/? c.1461C>T r.(=) p.(=)
?/? c.1527G>A r.(=) p.(=)
?/? c.1541C>T r.(?) p.(Ser514Leu)
?/? c.1606C>T r.(?) p.(Arg536Cys)
?/? c.1622G>A r.(?) p.(Arg541His)
?/? c.1623C>G r.(=) p.(=)
?/? c.1658A>G r.(?) p.(Lys553Arg)
?/? c.1723C>T r.(?) p.(Arg575Trp)
?/? c.1730T>G r.(?) p.(Ile577Ser)
?/? c.1751T>C r.(?) p.(Leu584Pro)
?/? c.1789G>A r.(?) p.(Val597Met)
?/? c.1821C>G r.(?) p.(Asn607Lys)
?/? c.1834T>G r.(?) p.(Tyr612Asp)
?/? c.1849C>T r.(?) p.(Arg617Cys)
?/? c.1855C>T r.(=) p.(=)
?/? c.1891C>T r.(?) p.(Gln631*)
?/? c.1894C>T r.(?) p.(Arg632Cys)
?/? c.1917G>C r.(?) p.(Lys639Asn)
?/? c.1939G>A r.(?) p.(Asp647Asn)
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