Transcript #00005626

Transcript name family with sequence similarity 47, member B
Gene name FAM47B (family with sequence similarity 47, member B)
Chromosome X
Transcript - NCBI ID NM_152631.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_689844.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

74 entries on 1 page. Showing entries 1 - 74.
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Affects function     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/? c.-17C>G r.(=) p.(=)
?/? c.-8G>C r.(=) p.(=)
?/? c.11G>A r.(?) p.(Arg4Gln)
?/? c.53A>C r.(?) p.(Lys18Thr)
?/? c.54G>A r.(=) p.(=)
?/? c.97C>T r.(?) p.(Arg33Cys)
?/? c.102G>A r.(=) p.(=)
?/? c.156G>A r.(=) p.(=)
?/? c.181G>A r.(?) p.(Ala61Thr)
?/? c.198A>G r.(=) p.(=)
?/? c.263C>T r.(?) p.(Ala88Val)
?/? c.289C>T r.(=) p.(=)
?/? c.303G>T r.(=) p.(=)
?/? c.315C>T r.(=) p.(=)
?/? c.341G>A r.(?) p.(Arg114Gln)
?/? c.348G>A r.(=) p.(=)
?/? c.358G>C r.(?) p.(Glu120Gln)
?/? c.416A>C r.(?) p.(Lys139Thr)
?/? c.466G>A r.(?) p.(Glu156Lys)
?/? c.475C>A r.(?) p.(Leu159Met)
?/? c.485C>A r.(?) p.(Ala162Asp)
?/? c.520G>C r.(?) p.(Glu174Gln)
?/? c.531C>T r.(=) p.(=)
?/? c.532G>T r.(?) p.(Glu178*)
?/? c.544T>C r.(?) p.(Tyr182His)
?/? c.618T>G r.(=) p.(=)
?/? c.631C>A r.(?) p.(Arg211Ser)
?/? c.647C>G r.(?) p.(Pro216Arg)
?/? c.744C>G r.(=) p.(=)
?/? c.766G>T r.(?) p.(Val256Leu)
?/? c.770C>A r.(?) p.(Ser257Tyr)
?/? c.840G>A r.(=) p.(=)
?/? c.855G>A r.(=) p.(=)
?/? c.864C>G r.(=) p.(=)
?/? c.890C>T r.(?) p.(Pro297Leu)
?/? c.899C>T r.(?) p.(Pro300Leu)
?/? c.915C>G r.(=) p.(=)
?/? c.923G>A r.(?) p.(Arg308His)
?/? c.954_955del r.(?) p.(Cys320Profs*34)
?/? c.1003C>G r.(?) p.(Pro335Ala)
?/? c.1018C>T r.(?) p.(Arg340Trp)
?/? c.1037T>G r.(?) p.(Leu346Arg)
?/? c.1088G>T r.(?) p.(Arg363Leu)
?/? c.1114G>A r.(?) p.(Glu372Lys)
?/? c.1129C>A r.(?) p.(Pro377Thr)
?/? c.1162C>T r.(?) p.(Arg388Trp)
?/? c.1238A>G r.(?) p.(Lys413Arg)
?/? c.1252C>G r.(?) p.(Arg418Gly)
?/? c.1256G>C r.(?) p.(Arg419Pro)
?/? c.1334G>A r.(?) p.(Ser445Asn)
?/? c.1341G>A r.(?) p.(Met447Ile)
?/? c.1369A>G r.(?) p.(Arg457Gly)
?/? c.1391G>A r.(?) p.(Arg464His)
?/? c.1404G>T r.(?) p.(Trp468Cys)
?/? c.1414C>G r.(?) p.(Leu472Val)
?/? c.1479T>C r.(=) p.(=)
?/? c.1487A>C r.(?) p.(Gln496Pro)
?/? c.1503A>T r.(=) p.(=)
?/? c.1506C>T r.(=) p.(=)
?/? c.1522C>T r.(=) p.(=)
?/? c.1607C>T r.(?) p.(Pro536Leu)
?/? c.1620T>C r.(=) p.(=)
?/? c.1635_1636insC r.(?) p.(Ile546Hisfs*11)
?/? c.1649C>T r.(?) p.(Pro550Leu)
?/? c.1664C>T r.(?) p.(Pro555Leu)
?/? c.1666A>C r.(?) p.(Lys556Gln)
?/? c.1761T>C r.(=) p.(=)
?/? c.1855G>A r.(?) p.(Asp619Asn)
?/? c.1863T>A r.(=) p.(=)
?/? c.1864A>G r.(?) p.(Lys622Glu)
?/? c.1891G>A r.(?) p.(Val631Ile)
?/? c.1928A>T r.(?) p.(Lys643Ile)
?/? c.*23A>C r.(=) p.(=)
?/? c.*46C>G r.(=) p.(=)
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