Transcript #00011601 (NM_021642.3, FCGR2A gene)

Transcript name transcript variant 2
Gene name FCGR2A (Fc fragment of IgG, low affinity IIa, receptor (CD32))
Chromosome 1
Transcript - NCBI ID NM_021642.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_067674.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

62 entries on 1 page. Showing entries 1 - 62.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

Position     

RNA change     

Protein     

PolyPhen prediction     

GVS function     

Splice distance     
./. - c.85+31T>C 85 r.(=) p.(=) - intron 31
./. - c.86-27G>A 86 r.(=) p.(=) - intron 27
./. - c.184C>T 184 r.(?) p.(Gln62Ter) - stop-gained -
./. - c.184C>T 184 r.(?) p.(Gln62Ter) - stop-gained -
./. - c.184C>T 184 r.(?) p.(Gln62Ter) - stop-gained -
./. - c.184C>T 184 r.(?) p.(Gln62Ter) - stop-gained -
./. - c.184C>T 184 r.(?) p.(Gln62Ter) - stop-gained -
./. - c.185A>G 185 r.(?) p.(Gln62Arg) - missense -
./. - c.185A>G 185 r.(?) p.(Gln62Arg) - missense -
./. - c.185A>G 185 r.(?) p.(Gln62Arg) - missense -
./. - c.333C>T 333 r.(?) p.(=) - coding-synonymous -
./. - c.362-11G>A 362 r.(=) p.(=) - intron 11
./. - c.362-11G>A 362 r.(=) p.(=) - intron 11
./. - c.362-11G>A 362 r.(=) p.(=) - intron 11
./. - c.362-11G>A 362 r.(=) p.(=) - intron 11
./. - c.362-11G>A 362 r.(=) p.(=) - intron 11
./. - c.362-11G>A 362 r.(=) p.(=) - intron 11
./. - c.362-11G>A 362 r.(=) p.(=) - intron 11
./. - c.497A>G 497 r.(?) p.(His166Arg) - missense -
./. - c.497A>G 497 r.(?) p.(His166Arg) - missense -
./. - c.497A>G 497 r.(?) p.(His166Arg) - missense -
./. - c.497A>G 497 r.(?) p.(His166Arg) - missense -
./. - c.497A>G 497 r.(?) p.(His166Arg) - missense -
./. - c.497A>G 497 r.(?) p.(His166Arg) - missense -
./. - c.497A>G 497 r.(?) p.(His166Arg) - missense -
./. - c.497A>G 497 r.(?) p.(His166Arg) - missense -
./. - c.497A>G 497 r.(?) p.(His166Arg) - missense -
./. - c.497A>G 497 r.(?) p.(His166Arg) - missense -
./. - c.497A>G 497 r.(?) p.(His166Arg) - missense -
./. - c.497A>G 497 r.(?) p.(His166Arg) - missense -
./. - c.497A>G 497 r.(?) p.(His166Arg) - missense -
./. - c.497A>G 497 r.(?) p.(His166Arg) - missense -
./. - c.497A>G 497 r.(?) p.(His166Arg) - missense -
./. - c.497A>G 497 r.(?) p.(His166Arg) - missense -
./. - c.497A>G 497 r.(?) p.(His166Arg) - missense -
./. - c.497A>G 497 r.(?) p.(His166Arg) - missense -
./. - c.497A>G 497 r.(?) p.(His166Arg) - missense -
./. - c.497A>G 497 r.(?) p.(His166Arg) - missense -
./. - c.497A>G 497 r.(?) p.(His166Arg) - missense -
./. - c.497A>G 497 r.(?) p.(His166Arg) - missense -
./. - c.642A>G 642 r.(?) p.(=) - coding-synonymous -
./. - c.642A>G 642 r.(?) p.(=) - coding-synonymous -
./. - c.739+17A>G 739 r.(=) p.(=) - intron 17
./. - c.740-29C>T 740 r.(=) p.(=) - intron 29
./. - c.777+28C>T 777 r.(=) p.(=) - intron 28
./. - c.777+383_*77824del 777 r.spl? p.? - - 383
./. - c.876C>T 876 r.(?) p.(=) - coding-synonymous -
./. - c.876C>T 876 r.(?) p.(=) - coding-synonymous -
./. - c.876C>T 876 r.(?) p.(=) - coding-synonymous -
./. - c.876C>T 876 r.(?) p.(=) - coding-synonymous -
./. - c.876C>T 876 r.(?) p.(=) - coding-synonymous -
./. - c.*79T>C 1030 r.(=) p.(=) - utr-3 -
./. - c.*79T>C 1030 r.(=) p.(=) - utr-3 -
./. - c.*79T>C 1030 r.(=) p.(=) - utr-3 -
./. - c.*79T>C 1030 r.(=) p.(=) - utr-3 -
./. - c.*79T>C 1030 r.(=) p.(=) - utr-3 -
./. - c.*79T>C 1030 r.(=) p.(=) - utr-3 -
./. - c.*79T>C 1030 r.(=) p.(=) - utr-3 -
./. - c.*79T>C 1030 r.(=) p.(=) - utr-3 -
./. - c.*79T>C 1030 r.(=) p.(=) - utr-3 -
./. - c.*79T>C 1030 r.(=) p.(=) - utr-3 -
./. - c.*79T>C 1030 r.(=) p.(=) - utr-3 -
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