Transcript #00014667 (NM_022162.1, NOD2 gene)

Transcript name nucleotide-binding oligomerization domain containing 2
Gene name NOD2 (nucleotide-binding oligomerization domain containing 2)
Chromosome 16
Transcript - NCBI ID NM_022162.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_071445.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.-58T>C r.(?) p.(=)
-?/. - c.2T>C r.(?) p.(Met1?)
-?/. - c.7G>C r.(?) p.(Glu3Gln)
-?/. - c.71C>T r.(?) p.(Pro24Leu)
-/. - c.74-29T>G r.(=) p.(=)
-?/. - c.74-7T>A r.(=) p.(=)
?/. - c.74-7T>A r.(=) p.(=)
-?/. - c.140C>T r.(?) p.(Ser47Leu)
?/. - c.140C>T r.(?) p.(Ser47Leu)
-?/. - c.140C>T r.(?) p.(Ser47Leu)
?/. - c.214G>A r.(?) p.(Glu72Lys)
-?/. - c.270C>T r.(?) p.(Asp90=)
-?/. - c.289A>G r.(?) p.(Thr97Ala)
-?/. - c.315G>A r.(?) p.(Ala105=)
-?/. - c.321C>G r.(?) p.(Ala107=)
-?/. - c.374C>T r.(?) p.(Pro125Leu)
?/. - c.404A>G r.(?) p.(Gln135Arg)
?/. - c.413G>A r.(?) p.(Arg138Gln)
-/. - c.418G>A r.(?) p.(Ala140Thr)
?/. - c.458T>G r.(?) p.(Leu153Arg)
-?/. - c.484G>A r.(?) p.(Val162Ile)
-/. - c.534C>G r.(?) p.(Ser178=)
-/. - c.534C>G r.(?) p.(Ser178=)
-/. - c.541-3T>C r.spl? p.?
-?/. - c.566C>T r.(?) p.(Thr189Met)
-?/. - c.566C>T r.(?) p.(Thr189Met)
-?/. - c.566C>T r.(?) p.(Thr189Met)
-?/. - c.567G>A r.(?) p.(Thr189=)
-?/. - c.567G>A r.(?) p.(Thr189=)
-?/. - c.580G>C r.(?) p.(Gly194Arg)
?/. - c.619C>G r.(?) p.(Pro207Ala)
-/. - c.633C>T r.(?) p.(Ala211=)
?/. - c.646+1G>A r.spl? p.?
?/. - c.743T>G r.(?) p.(Leu248Arg)
./. - c.743T>G r.(?) p.(Leu248Arg)
?/. - c.746A>G r.(?) p.(Glu249Gly)
?/. - c.746A>G r.(?) p.(Glu249Gly)
?/. - c.746A>G r.(?) p.(Glu249Gly)
?/. - c.772G>C r.(?) p.(Glu258Gln)
-/. - c.802C>T r.(?) p.(Pro268Ser)
-/. - c.802C>T r.(?) p.(Pro268Ser)
-?/. - c.816C>T r.(?) p.(Ser272=)
?/. - c.859C>T r.(?) p.(His287Tyr)
-?/. - c.866A>G r.(?) p.(Asn289Ser)
-/. - c.866A>G r.(?) p.(Asn289Ser)
-?/. - c.881C>G r.(?) p.(Thr294Ser)
-?/. - c.881C>G r.(?) p.(Thr294Ser)
-?/. - c.930G>A r.(?) p.(Gln310=)
?/. - c.931C>T r.(?) p.(Arg311Trp)
?/. - c.931C>T r.(?) p.(Arg311Trp)
?/. - c.931C>T r.(?) p.(Arg311Trp)
-?/. - c.931C>T r.(?) p.(Arg311Trp)
-?/. - c.932G>A r.(?) p.(Arg311Gln)
+/. - c.1000C>T r.(?) p.(Arg334Trp)
+/. - c.1000C>T r.(?) p.(Arg334Trp)
+/. - c.1001G>A r.(?) p.(Arg334Gln)
+/. - c.1001G>A r.(?) p.(Arg334Gln)
?/. - c.1022A>C r.(?) p.(Lys341Thr)
?/. - c.1036C>T r.(?) p.(Arg346Trp)
-/. - c.1055A>G r.(?) p.(His352Arg)
-?/. - c.1070A>C r.(?) p.(Asp357Ala)
?/. - c.1087A>T r.(?) p.(Ile363Phe)
?/. - c.1102C>T r.(?) p.(Leu368Phe)
?/. - c.1117C>T r.(?) p.(Arg373Cys)
?/. - c.1117C>T r.(?) p.(Arg373Cys)
?/. 1 c. 1118G>A r.(?) p.(Arg373His)
+/. - c.1147G>C r.(?) p.(Glu383Gln)
+/. - c.1148A>G r.(?) p.(Glu383Gly)
?/. - c.1169A>T r.(?) p.(Asp390Val)
?/. - c.1169A>T r.(?) p.(Asp390Val)
?/. - c.1169A>T r.(?) p.(Asp390Val)
-?/. - c.1194C>T r.(?) p.(Thr398=)
?/. - c.1195G>A r.(?) p.(Asp399Asn)
-?/. - c.1269G>T r.(?) p.(Val423=)
-?/. - c.1269G>T r.(?) p.(Val423=)
-?/. - c.1281G>C r.(?) p.(Pro427=)
?/. - c.1292C>T r.(?) p.(Ser431Leu)
-?/. - c.1292C>T r.(?) p.(Ser431Leu)
-?/. - c.1292C>T r.(?) p.(Ser431Leu)
-?/. - c.1292C>T r.(?) p.(Ser431Leu)
?/. - c.1295C>T r.(?) p.(Ala432Val)
?/. - c.1295C>T r.(?) p.(Ala432Val)
?/. - c.1321G>A r.(?) p.(Glu441Lys)
?/. - c.1321G>A r.(?) p.(Glu441Lys)
-/. - c.1377C>T r.(?) p.(Arg459=)
-/. - c.1377C>T r.(?) p.(Arg459=)
-?/. - c.1411C>T r.(?) p.(Arg471Cys)
-?/. - c.1411C>T r.(?) p.(Arg471Cys)
-/. - c.1453C>T r.(?) p.(Leu485=)
+/. - c.1496T>A r.(?) p.(Leu499Gln)
?/. - c.1502T>C r.(?) p.(Leu501Pro)
?/. - c.1515del r.(?) p.(Ser506Profs*11)
?/. - c.1531A>G r.(?) p.(Thr511Ala)
+/. - c.1538T>C r.(?) p.(Met513Thr)
+/. - c.1538T>C r.(?) p.(Met513Thr)
-?/. - c.1644G>A r.(?) p.(Leu548=)
-?/. - c.1752C>T r.(?) p.(=)
-/. - c.1761T>G r.(?) p.(Arg587=)
-/. - c.1761T>G r.(?) p.(Arg587=)
-?/. - c.1773C>T r.(?) p.(Val591=)
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