Transcript #00007763 (NM_032447.3, FBN3 gene)

Transcript name fibrillin 3
Gene name FBN3 (fibrillin 3)
Chromosome 19
Transcript - NCBI ID NM_032447.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_115823.3
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

70 entries on 1 page. Showing entries 1 - 70.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-/. - c.102C>T r.(?) p.(Asp34=)
+?/. 1 c.143G>A r.(143g>a) p.(Arg48Gln)
-/. - c.349+6C>T r.(=) p.(=)
-/. - c.349+14G>A r.(=) p.(=)
-?/. - c.356G>C r.(?) p.(Gly119Ala)
?/. - c.445+3_445+6del r.spl? p.?
?/. - c.647G>A r.(?) p.(Arg216His)
-?/. - c.716A>G r.(?) p.(Asn239Ser)
-/. - c.986C>T r.(?) p.(Pro329Leu)
-?/. - c.1060C>A r.(?) p.(Pro354Thr)
?/. 10 c.1234T>C r.(?) p.(Cys412Arg)
-?/. - c.1332C>T r.(?) p.(Arg444=)
-/. - c.1345+6C>A r.(=) p.(=)
?/. - c.1381G>A r.(?) p.(Gly461Ser)
-?/. - c.1466-6C>T r.(=) p.(=)
-?/. - c.1591+7T>G r.(=) p.(=)
-/. - c.1591+13T>G r.(=) p.(=)
-/. - c.1591+17C>G r.(=) p.(=)
-/. - c.1599C>T r.(?) p.(Asn533=)
-/. - c.1624G>A r.(?) p.(Val542Ile)
-/. - c.1714+3G>A r.spl? p.?
-/. - c.1785C>T r.(?) p.(Arg595=)
?/. - c.1808C>A r.(?) p.(Ala603Glu)
-/. - c.1920C>G r.(?) p.(Ser640=)
-/. - c.1984G>A r.(?) p.(Asp662Asn)
-/. - c.2505C>T r.(?) p.(Cys835=)
-/. - c.2555-17T>C r.(=) p.(=)
-/. - c.2555-7G>A r.(=) p.(=)
-/. - c.2602G>A r.(?) p.(Asp868Asn)
?/. - c.2941C>G r.(?) p.(Arg981Gly)
?/. - c.2942G>A r.(?) p.(Arg981Gln)
-/. - c.3083-12dup r.(=) p.(=)
?/. - c.3104C>T r.(?) p.(Ser1035Phe)
-/. - c.3877A>G r.(?) p.(Ser1293Gly)
-/. - c.3903G>A r.(?) p.(Pro1301=)
-/. - c.3976G>A r.(?) p.(Val1326Ile)
-/. - c.4047C>T r.(?) p.(Cys1349=)
-/. - c.4143G>A r.(?) p.(Ala1381=)
?/. - c.4199G>A r.(?) p.(Arg1400Gln)
-/. - c.4334-13T>C r.(=) p.(=)
-/. - c.4456+4A>G r.spl? p.?
?/. - c.4462C>T r.(?) p.(Arg1488Trp)
?/. - c.4745C>T r.(?) p.(Thr1582Met)
?/. - c.4754G>T r.(?) p.(Ser1585Ile)
-/. - c.4840G>A r.(?) p.(Gly1614Ser)
?/. - c.4847G>A r.(?) p.(Cys1616Tyr)
-/. - c.5089+18A>G r.(=) p.(=)
-/. - c.5090-12C>T r.(=) p.(=)
?/. - c.5343C>G r.(?) p.(Ile1781Met)
-/. - c.5417G>A r.(?) p.(Arg1806Gln)
-/. - c.5607C>G r.(?) p.(Asn1869Lys)
-/. - c.5710C>T r.(?) p.(Leu1904Phe)
-/. - c.5826C>A r.(?) p.(Pro1942=)
-/. - c.5873C>A r.(?) p.(Pro1958His)
-/. - c.5896C>G r.(?) p.(His1966Asp)
-/. - c.6177G>A r.(?) p.(Glu2059=)
-/. - c.6250+18A>G r.(=) p.(=)
-/. - c.6603T>C r.(?) p.(Asp2201=)
?/. - c.6604G>A r.(?) p.(Gly2202Arg)
?/. - c.6832G>C r.(?) p.(Asp2278His)
-?/. - c.7360C>A r.(?) p.(Gln2454Lys)
-/. - c.7419G>A r.(?) p.(Pro2473=)
?/. - c.7498G>A r.(?) p.(Gly2500Arg)
-/. - c.7620T>G r.(?) p.(His2540Gln)
?/. - c.7780G>A r.(?) p.(Val2594Ile)
-?/. - c.7780G>A r.(?) p.(Val2594Ile)
-/. - c.7830G>T r.(?) p.(Glu2610Asp)
-/. - c.7938-20C>A r.(=) p.(=)
?/. - c.8366C>A r.(?) p.(Pro2789Gln)
-?/. - c.8366C>A r.(?) p.(Pro2789Gln)
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