Transcript #00005544

Transcript name fatty acid amide hydrolase 2
Gene name FAAH2 (fatty acid amide hydrolase 2)
Chromosome X
Transcript - NCBI ID NM_174912.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_777572.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

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

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/? c.-20C>T r.(=) p.(=)
?/? c.47C>A r.(?) p.(Ala16Glu)
?/? c.99T>C r.(=) p.(=)
?/? c.124C>T r.(?) p.(Arg42Trp)
?/? c.126G>C r.(=) p.(=)
?/? c.170C>T r.(?) p.(Ala57Val)
?/? c.192+47G>A r.(=) p.(=)
?/? c.193-24T>A r.(=) p.(=)
?/? c.198A>T r.(?) p.(Lys66Asn)
?/? c.222T>C r.(=) p.(=)
?/? c.241G>A r.(?) p.(Val81Met)
?/? c.275+30T>C r.(=) p.(=)
?/? c.276-21C>T r.(=) p.(=)
?/? c.276-16del r.(=) p.(=)
?/? c.276-8C>A r.(=) p.(=)
?/? c.283G>A r.(?) p.(Glu95Lys)
?/? c.288G>A r.(=) p.(=)
?/? c.412+31T>C r.(=) p.(=)
?/? c.413-38T>G r.(=) p.(=)
?/? c.413-16T>C r.(=) p.(=)
?/? c.419C>T r.(?) p.(Pro140Leu)
?/? c.425C>A r.(?) p.(Ser142Tyr)
?/? c.426T>C r.(=) p.(=)
?/? c.442C>T r.(?) p.(Arg148Cys)
?/? c.443G>A r.(?) p.(Arg148His)
?/? c.448G>A r.(?) p.(Asp150Asn)
?/? c.452C>T r.(?) p.(Ala151Val)
?/? c.464C>T r.(?) p.(Thr155Ile)
?/? c.526T>C r.(?) p.(Cys176Arg)
?/? c.527G>A r.(?) p.(Cys176Tyr)
?/? c.575G>A r.(?) p.(Arg192Gln)
?/? c.607G>T r.(?) p.(Val203Leu)
?/? c.622G>A r.(?) p.(Gly208Ser)
?/? c.623-30T>G r.(=) p.(=)
?/? c.623-20G>A r.(=) p.(=)
?/? c.623-12T>C r.(=) p.(=)
?/? c.623-10del r.(=) p.(=)
?/? c.625G>A r.(?) p.(Gly209Ser)
?/? c.656C>G r.(?) p.(Ser219*)
?/? c.663T>C r.(=) p.(=)
?/? c.716G>T r.(?) p.(Gly239Val)
?/? c.739C>T r.(?) p.(Pro247Ser)
?/? c.742+13T>C r.(=) p.(=)
?/? c.742+48G>A r.(=) p.(=)
?/? c.743-39C>A r.(=) p.(=)
?/? c.743-27G>A r.(=) p.(=)
?/? c.780G>A r.(=) p.(=)
?/? c.781G>C r.(?) p.(Gly261Arg)
?/? c.795G>T r.(?) p.(Leu265Phe)
?/? c.820C>T r.(?) p.(Arg274Cys)
?/? c.822T>C r.(=) p.(=)
?/? c.838G>T r.(?) p.(Ala280Ser)
?/? c.869G>A r.(?) p.(Gly290Glu)
?/? c.879-27T>C r.(=) p.(=)
?/? c.936T>C r.(=) p.(=)
?/? c.943G>A r.(?) p.(Gly315Ser)
?/? c.945C>A r.(=) p.(=)
?/? c.962A>G r.(?) p.(Lys321Arg)
?/? c.967G>C r.(?) p.(Asp323His)
?/? c.997-25T>C r.(=) p.(=)
?/? c.1029C>T r.(=) p.(=)
?/? c.1059G>A r.(?) p.(Met353Ile)
?/? c.1084G>A r.(?) p.(Ala362Thr)
?/? c.1103G>A r.(?) p.(Gly368Glu)
?/? c.1116+11C>T r.(=) p.(=)
?/? c.1116+27T>A r.(=) p.(=)
?/? c.1117-47A>G r.(=) p.(=)
?/? c.1117-40G>C r.(=) p.(=)
?/? c.1117G>A r.(?) p.(Glu373Lys)
?/? c.1140G>C r.(?) p.(Leu380Phe)
?/? c.1151A>T r.(?) p.(His384Leu)
?/? c.1179G>A r.(=) p.(=)
?/? c.1228+4T>C r.spl? p.?
?/? c.1228+17C>T r.(=) p.(=)
?/? c.1228+34A>T r.(=) p.(=)
?/? c.1229-27A>G r.(=) p.(=)
?/? c.1229-18T>C r.(=) p.(=)
?/? c.1229-14A>T r.(=) p.(=)
?/? c.1239G>A r.(=) p.(=)
?/? c.1294G>T r.(?) p.(Glu432*)
?/? c.1333G>C r.(?) p.(Asp445His)
?/? c.1355C>T r.(?) p.(Pro452Leu)
?/? c.1372G>A r.(?) p.(Ala458Thr)
?/? c.1398A>T r.(=) p.(=)
?/? c.1404T>C r.(=) p.(=)
?/? c.1424-50T>G r.(=) p.(=)
?/? c.1424-38G>T r.(=) p.(=)
?/? c.1424-6C>A r.(=) p.(=)
?/? c.1447C>T r.(?) p.(Pro483Ser)
?/? c.1463C>G r.(?) p.(Pro488Arg)
?/? c.1467G>A r.(=) p.(=)
?/? c.1480del r.(?) p.(Gly495Aspfs*4)
?/? c.1483G>A r.(?) p.(Gly495Arg)
?/? c.1518C>T r.(=) p.(=)
?/? c.1520T>G r.(?) p.(Phe507Cys)
?/? c.1523A>G r.(?) p.(Asn508Ser)
?/? c.1529A>T r.(?) p.(His510Leu)
?/? c.1553A>G r.(?) p.(Tyr518Cys)
?/? c.1573G>A r.(?) p.(Gly525Ser)
?/? c.1583G>C r.(?) p.(Cys528Ser)
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