Transcript #00001098 (NM_003890.2, FCGBP gene)

Transcript name Fc fragment of IgG binding protein
Gene name FCGBP (Fc fragment of IgG binding protein)
Chromosome 19
Transcript - NCBI ID NM_003890.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_003881.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2012-09-13 13:12:32 +02:00 (CEST)
Date last edited N/A


Variants

60 entries on 1 page. Showing entries 1 - 60.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.401G>A r.(?) p.(Arg134Gln)
-?/. - c.554A>G r.(?) p.(Tyr185Cys)
?/. - c.687G>A r.(=) p.(=)
-?/. - c.1069G>A r.(?) p.(Val357Met)
-?/. - c.1138A>C r.(?) p.(Lys380Gln)
?/. - c.1464C>A r.(?) p.(Tyr488*)
-?/. - c.1851C>T r.(?) p.(Asp617=)
-?/. - c.1878C>T r.(?) p.(Asp626=)
?/. - c.2012A>C r.(?) p.(Asp671Ala)
?/. - c.2615A>G r.(?) p.(Tyr872Cys)
-?/. - c.2897G>T r.(?) p.(Gly966Val)
-?/. - c.2995C>G r.(?) p.(Leu999Val)
-?/. - c.3114C>T r.(?) p.(Pro1038=)
-?/. - c.3404G>A r.(?) p.(Ser1135Asn)
?/. - c.3499C>T r.(?) p.(His1167Tyr)
?/. - c.3739G>A r.(?) p.(Val1247Met)
-?/. - c.3847G>A r.(?) p.(Gly1283Ser)
-?/. - c.4221A>G r.(?) p.(Ser1407=)
?/. - c.4554C>G r.(?) p.(His1518Gln)
?/. - c.4585C>T r.(?) p.(Pro1529Ser)
?/. - c.4585C>T r.(?) p.(Pro1529Ser)
?/. - c.4775T>C r.(?) p.(Val1592Ala)
?/. - c.4918G>C r.(?) p.(Val1640Leu)
?/. - c.4927+1G>A r.spl? p.?
?/. - c.4927+1558T>G r.(=) p.(=)
?/. - c.4927+1576G>A r.(=) p.(=)
-?/. - c.5059C>T r.(?) p.(Arg1687Trp)
-?/. - c.6606G>A r.(?) p.(Ala2202=)
?/. - c.7120G>A r.(?) p.(Asp2374Asn)
?/. - c.7849G>C r.(?) p.(Gly2617Arg)
?/. - c.7963_7965del r.(?) p.(Lys2655del)
-?/. - c.8174A>C r.(?) p.(Asn2725Thr)
?/. - c.8360G>A r.(?) p.(Gly2787Asp)
?/. - c.8451_8453del r.(?) p.(Val2819del)
?/. - c.8480C>T r.(?) p.(Pro2827Leu)
-?/. - c.9238G>A r.(?) p.(Gly3080Arg)
?/. - c.9485C>T r.(?) p.(Pro3162Leu)
?/. - c.10186G>C r.(?) p.(Val3396Leu)
-?/. - c.11435G>A r.(?) p.(Gly3812Asp)
-?/. - c.11531del r.(?) p.(Ile3844Thrfs*43)
-?/. - c.11538C>G r.(?) p.(Ser3846Arg)
-?/. - c.11548C>T r.(?) p.(Pro3850Ser)
?/. - c.11566_11568del r.(?) p.(Lys3856del)
?/. - c.11760C>G r.(?) p.(His3920Gln)
-?/. - c.11777A>C r.(?) p.(Asn3926Thr)
?/. - c.11791C>T r.(?) p.(Pro3931Ser)
?/. - c.11803C>T r.(?) p.(Pro3935Ser)
?/. - c.12124G>C r.(?) p.(Val4042Leu)
-?/. - c.12848_12855del r.(?) p.(Leu4283ArgfsTer16)
-?/. - c.13296G>C r.(?) p.(Gln4432His)
-?/. - c.13914G>C r.(?) p.(Gly4638=)
-?/. - c.13987G>A r.(?) p.(Gly4663Ser)
?/. - c.14413G>A r.(?) p.(Glu4805Lys)
?/. - c.14515T>C r.(?) p.(Cys4839Arg)
-?/. - c.14691C>T r.(?) p.(Ile4897=)
-?/. - c.15055G>A r.(?) p.(Gly5019Ser)
-?/. - c.15078G>C r.(?) p.(Glu5026Asp)
-?/. - c.15124G>T r.(?) p.(Ala5042Ser)
?/. - c.15124G>T r.(?) p.(Ala5042Ser)
-?/. - c.15631G>A r.(?) p.(Ala5211Thr)
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