Transcript #00023397 (NM_001002275.2, FCGR2B gene)

Transcript name Manually created transcript
Gene name FCGR2B (Fc fragment of IgG, low affinity IIb, receptor (CD32))
Chromosome 1
Transcript - NCBI ID NM_001002275.2
Transcript - Ensembl ID -
Protein - NCBI ID -
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

47 entries on 1 page. Showing entries 1 - 47.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

Position     

RNA change     

Protein     

PolyPhen prediction     

GVS function     

Splice distance     
./. - c.186G>A 186 r.(?) p.(=) - coding-synonymous -
./. - c.216G>A 216 r.(?) p.(=) - coding-synonymous -
./. - c.333G>A 333 r.(?) p.(=) - coding-synonymous -
./. - c.333G>A 333 r.(?) p.(=) - coding-synonymous -
./. - c.333G>A 333 r.(?) p.(=) - coding-synonymous -
./. - c.333G>A 333 r.(?) p.(=) - coding-synonymous -
./. - c.333G>A 333 r.(?) p.(=) - coding-synonymous -
./. - c.333G>A 333 r.(?) p.(=) - coding-synonymous -
./. - c.333G>A 333 r.(?) p.(=) - coding-synonymous -
./. - c.333G>A 333 r.(?) p.(=) - coding-synonymous -
./. - c.333G>A 333 r.(?) p.(=) - coding-synonymous -
./. - c.609G>A 609 r.(?) p.(=) - coding-synonymous -
./. - c.609G>A 609 r.(?) p.(=) - coding-synonymous -
./. - c.609G>A 609 r.(?) p.(=) - coding-synonymous -
./. - c.609G>A 609 r.(?) p.(=) - coding-synonymous -
./. - c.609G>A 609 r.(?) p.(=) - coding-synonymous -
./. - c.609G>A 609 r.(?) p.(=) - coding-synonymous -
./. - c.643+6C>A 643 r.(=) p.(=) - splice 6
./. - c.643+6C>A 643 r.(=) p.(=) - splice 6
./. - c.643+6C>A 643 r.(=) p.(=) - splice 6
./. - c.643+6C>A 643 r.(=) p.(=) - splice 6
./. - c.643+6C>A 643 r.(=) p.(=) - splice 6
./. - c.692T>C 692 r.(?) p.(Ile231Thr) - missense -
./. - c.692T>C 692 r.(?) p.(Ile231Thr) - missense -
./. - c.692T>C 692 r.(?) p.(Ile231Thr) - missense -
./. - c.692T>C 692 r.(?) p.(Ile231Thr) - missense -
./. - c.692T>C 692 r.(?) p.(Ile231Thr) - missense -
./. - c.692T>C 692 r.(?) p.(Ile231Thr) - missense -
./. - c.692T>C 692 r.(?) p.(Ile231Thr) - missense -
./. - c.692T>C 692 r.(?) p.(Ile231Thr) - missense -
./. - c.692T>C 692 r.(?) p.(Ile231Thr) - missense -
./. - c.692T>C 692 r.(?) p.(Ile231Thr) - missense -
./. - c.692T>C 692 r.(?) p.(Ile231Thr) - missense -
./. - c.692T>C 692 r.(?) p.(Ile231Thr) - missense -
./. - c.692T>C 692 r.(?) p.(Ile231Thr) - missense -
./. - c.758-37C>A 758 r.(=) p.(=) - intron 37
./. - c.758-37C>A 758 r.(=) p.(=) - intron 37
./. - c.758-37C>A 758 r.(=) p.(=) - intron 37
./. - c.758-37C>A 758 r.(=) p.(=) - intron 37
./. - c.758-37C>A 758 r.(=) p.(=) - intron 37
./. - c.758-37C>A 758 r.(=) p.(=) - intron 37
./. - c.758-37C>A 758 r.(=) p.(=) - intron 37
./. - c.758-37C>A 758 r.(=) p.(=) - intron 37
./. - c.758-37C>A 758 r.(=) p.(=) - intron 37
./. - c.763C>T 763 r.(?) p.(Pro255Ser) - missense -
./. - c.769T>G 769 r.(?) p.(Tyr257Asp) - missense -
./. - c.*17T>C 947 r.(=) p.(=) - utr-3 -
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