Transcript #00025605 (NM_003839.3, TNFRSF11A gene)

Transcript name transcript variant 1
Gene name TNFRSF11A (tumor necrosis factor receptor superfamily, member 11a, NFKB activator)
Chromosome 18
Transcript - NCBI ID NM_003839.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_003830.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2021-03-22 10:13:45 +01:00 (CET)
Date last edited N/A


Variants

68 entries on 1 page. Showing entries 1 - 68.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+/. - c.-11629922_*17962913del r.0? p.0?
-?/. - c.75+5G>A r.spl? p.?
-/. - c.75+5G>A r.spl? p.?
-?/. - c.102T>C r.(?) p.(Cys34=)
-?/. - c.109G>A r.(?) p.(Glu37Lys)
?/. - c.109G>A r.(?) p.(Glu37Lys)
-?/. - c.109G>A r.(?) p.(Glu37Lys)
-?/. - c.158-34T>G r.(=) p.(=)
-?/. - c.283+8C>T r.(=) p.(=)
?/. - c.284-5C>A r.spl? p.?
-/. - c.284-5C>T r.spl? p.?
-?/. - c.327C>T r.(?) p.(Pro109=)
-?/. - c.327C>T r.(?) p.(Pro109=)
+/. - c.328dup r.(?) p.(Arg110ProfsTer52)
+/. - c.330del r.(?) p.(Arg111AlafsTer72)
+?/. - c.400G>A r.(?) p.(Ala134Thr)
-?/. - c.428-20T>G r.(=) p.(=)
-/. - c.428-9T>C r.(=) p.(=)
-?/. - c.428-9_428-8del r.(=) p.(=)
-/. - c.428-8del r.(=) p.(=)
-?/. - c.428-8del r.(=) p.(=)
-/. - c.428-8dup r.(=) p.(=)
-/. - c.522-17C>T r.(=) p.(=)
-?/. - c.543A>T r.(?) p.(Arg181Ser)
-/. - c.570C>T r.(?) p.(Ser190=)
-/. - c.575C>T r.(?) p.(Ala192Val)
?/. - c.633G>T r.(?) p.(Leu211Phe)
-?/. - c.636C>T r.(?) p.(Pro212=)
?/. - c.718A>G r.(?) p.(Lys240Glu)
?/. - c.718A>G r.(?) p.(Lys240Glu)
-?/. - c.718A>G r.(?) p.(Lys240Glu)
-?/. - c.730+5T>C r.spl? p.?
-?/. - c.730+6G>C r.(=) p.(=)
-?/. - c.748A>G r.(?) p.(Ile250Val)
?/. - c.784G>C r.(?) p.(Glu262Gln)
-?/. - c.828T>C r.(?) p.(Phe276=)
-?/. - c.859C>T r.(?) p.(Leu287=)
-/. - c.933A>G r.(?) p.(Thr311=)
-?/. - c.955G>A r.(?) p.(Ala319Thr)
-?/. - c.986T>C r.(?) p.(Leu329Ser)
-?/. - c.1279G>A r.(?) p.(Asp427Asn)
?/. - c.1279G>A r.(?) p.(Asp427Asn)
-?/. - c.1348C>T r.(?) p.(Arg450Trp)
-?/. - c.1348C>T r.(?) p.(Arg450Trp)
+/. - c.1371_1372del r.(?) p.(Cys457*)
-/. - c.1381G>A r.(?) p.(Val461Met)
-?/. - c.1381G>A r.(?) p.(Val461Met)
-?/. - c.1397G>A r.(?) p.(Arg466His)
-?/. - c.1417G>A r.(?) p.(Ala473Thr)
?/. - c.1448_1450del r.(?) p.(Glu483del)
-?/. - c.1479C>T r.(?) p.(Pro493=)
-?/. - c.1515G>A r.(?) p.(Ala505=)
-?/. - c.1519G>A r.(?) p.(Ala507Thr)
-?/. - c.1519G>A r.(?) p.(Ala507Thr)
-?/. - c.1567+7G>A r.(=) p.(=)
-?/. - c.1618A>G r.(?) p.(Met540Val)
?/. - c.1618A>G r.(?) p.(Met540Val)
?/. - c.1618A>G r.(?) p.(Met540Val)
?/. - c.1618A>G r.(?) p.(Met540Val)
?/. - c.1683_1685dup r.(?) p.(Ala563dup)
?/. - c.1696A>T r.(?) p.(Met566Leu)
-?/. - c.1703G>A r.(?) p.(Arg568His)
?/. - c.1735G>T r.(?) p.(Asp579Tyr)
-?/. - c.1763T>C r.(?) p.(Phe588Ser)
?/. - c.1766C>G r.(?) p.(Pro589Arg)
-?/. - c.1776C>T r.(?) p.(Cys592=)
?/. - c.1804G>C r.(?) p.(Glu602Gln)
-?/. - c.1815G>A r.(?) p.(Ser605=)
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