Transcript #00011600 (NM_001136219.1, FCGR2A gene)

Transcript name transcript variant 1
Gene name FCGR2A (Fc fragment of IgG, low affinity IIa, receptor (CD32))
Chromosome 1
Transcript - NCBI ID NM_001136219.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001129691.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

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.187C>T 187 r.(?) p.(Gln63Ter) - stop-gained -
./. - c.187C>T 187 r.(?) p.(Gln63Ter) - stop-gained -
./. - c.187C>T 187 r.(?) p.(Gln63Ter) - stop-gained -
./. - c.187C>T 187 r.(?) p.(Gln63Ter) - stop-gained -
./. - c.187C>T 187 r.(?) p.(Gln63Ter) - stop-gained -
./. - c.188A>G 188 r.(?) p.(Gln63Arg) - missense -
./. - c.188A>G 188 r.(?) p.(Gln63Arg) - missense -
./. - c.188A>G 188 r.(?) p.(Gln63Arg) - missense -
./. - c.336C>T 336 r.(?) p.(=) - coding-synonymous -
./. - c.365-11G>A 365 r.(=) p.(=) - intron 11
./. - c.365-11G>A 365 r.(=) p.(=) - intron 11
./. - c.365-11G>A 365 r.(=) p.(=) - intron 11
./. - c.365-11G>A 365 r.(=) p.(=) - intron 11
./. - c.365-11G>A 365 r.(=) p.(=) - intron 11
./. - c.365-11G>A 365 r.(=) p.(=) - intron 11
./. - c.365-11G>A 365 r.(=) p.(=) - intron 11
./. - c.500A>G 500 r.(?) p.(His167Arg) - missense -
./. - c.500A>G 500 r.(?) p.(His167Arg) - missense -
./. - c.500A>G 500 r.(?) p.(His167Arg) - missense -
./. - c.500A>G 500 r.(?) p.(His167Arg) - missense -
./. - c.500A>G 500 r.(?) p.(His167Arg) - missense -
./. - c.500A>G 500 r.(?) p.(His167Arg) - missense -
./. - c.500A>G 500 r.(?) p.(His167Arg) - missense -
./. - c.500A>G 500 r.(?) p.(His167Arg) - missense -
./. - c.500A>G 500 r.(?) p.(His167Arg) - missense -
./. - c.500A>G 500 r.(?) p.(His167Arg) - missense -
./. - c.500A>G 500 r.(?) p.(His167Arg) - missense -
./. - c.500A>G 500 r.(?) p.(His167Arg) - missense -
./. - c.500A>G 500 r.(?) p.(His167Arg) - missense -
./. - c.500A>G 500 r.(?) p.(His167Arg) - missense -
./. - c.500A>G 500 r.(?) p.(His167Arg) - missense -
./. - c.500A>G 500 r.(?) p.(His167Arg) - missense -
./. - c.500A>G 500 r.(?) p.(His167Arg) - missense -
./. - c.500A>G 500 r.(?) p.(His167Arg) - missense -
./. - c.500A>G 500 r.(?) p.(His167Arg) - missense -
./. - c.500A>G 500 r.(?) p.(His167Arg) - missense -
./. - c.500A>G 500 r.(?) p.(His167Arg) - missense -
./. - c.500A>G 500 r.(?) p.(His167Arg) - missense -
./. - c.645A>G 645 r.(?) p.(=) - coding-synonymous -
./. - c.645A>G 645 r.(?) p.(=) - coding-synonymous -
./. - c.742+17A>G 742 r.(=) p.(=) - intron 17
./. - c.743-29C>T 743 r.(=) p.(=) - intron 29
./. - c.780+28C>T 780 r.(=) p.(=) - intron 28
./. - c.780+383_*77824del 780 r.spl? p.? - - 383
./. - c.879C>T 879 r.(?) p.(=) - coding-synonymous -
./. - c.879C>T 879 r.(?) p.(=) - coding-synonymous -
./. - c.879C>T 879 r.(?) p.(=) - coding-synonymous -
./. - c.879C>T 879 r.(?) p.(=) - coding-synonymous -
./. - c.879C>T 879 r.(?) p.(=) - coding-synonymous -
./. - c.*79T>C 1033 r.(=) p.(=) - utr-3 -
./. - c.*79T>C 1033 r.(=) p.(=) - utr-3 -
./. - c.*79T>C 1033 r.(=) p.(=) - utr-3 -
./. - c.*79T>C 1033 r.(=) p.(=) - utr-3 -
./. - c.*79T>C 1033 r.(=) p.(=) - utr-3 -
./. - c.*79T>C 1033 r.(=) p.(=) - utr-3 -
./. - c.*79T>C 1033 r.(=) p.(=) - utr-3 -
./. - c.*79T>C 1033 r.(=) p.(=) - utr-3 -
./. - c.*79T>C 1033 r.(=) p.(=) - utr-3 -
./. - c.*79T>C 1033 r.(=) p.(=) - utr-3 -
./. - c.*79T>C 1033 r.(=) p.(=) - utr-3 -
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