Transcript #00007220 (NM_000340.1, SLC2A2 gene)

Transcript name solute carrier family 2 (facilitated glucose transporter), member 2
Gene name SLC2A2 (solute carrier family 2 (facilitated glucose transporter), member 2)
Chromosome 3
Transcript - NCBI ID NM_000340.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_000331.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2013-10-30 13:00:19 +01:00 (CET)
Date last edited N/A


Variants

59 entries on 1 page. Showing entries 1 - 59.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

Position     

RNA change     

Protein     

PolyPhen prediction     

GVS function     

Splice distance     
./. - c.329C>T 329 r.(?) p.(Thr110Ile) - missense -
./. - c.329C>T 329 r.(?) p.(Thr110Ile) - missense -
./. - c.329C>T 329 r.(?) p.(Thr110Ile) - missense -
./. - c.329C>T 329 r.(?) p.(Thr110Ile) - missense -
./. - c.329C>T 329 r.(?) p.(Thr110Ile) - missense -
./. - c.329C>T 329 r.(?) p.(Thr110Ile) - missense -
./. - c.329C>T 329 r.(?) p.(Thr110Ile) - missense -
./. - c.329C>T 329 r.(?) p.(Thr110Ile) - missense -
./. - c.329C>T 329 r.(?) p.(Thr110Ile) - missense -
./. - c.329C>T 329 r.(?) p.(Thr110Ile) - missense -
./. - c.329C>T 329 r.(?) p.(Thr110Ile) - missense -
./. - c.594G>A 594 r.(?) p.(=) - coding-synonymous -
./. - c.594G>A 594 r.(?) p.(=) - coding-synonymous -
./. - c.594G>A 594 r.(?) p.(=) - coding-synonymous -
./. - c.594G>A 594 r.(?) p.(=) - coding-synonymous -
./. - c.594G>A 594 r.(?) p.(=) - coding-synonymous -
./. - c.594G>A 594 r.(?) p.(=) - coding-synonymous -
./. - c.594G>A 594 r.(?) p.(=) - coding-synonymous -
./. - c.594G>A 594 r.(?) p.(=) - coding-synonymous -
./. - c.776-15C>T 776 r.(=) p.(=) - intron 15
./. - c.776-15C>T 776 r.(=) p.(=) - intron 15
./. - c.776-15C>T 776 r.(=) p.(=) - intron 15
./. - c.776-15C>T 776 r.(=) p.(=) - intron 15
./. - c.776-15C>T 776 r.(=) p.(=) - intron 15
./. - c.776-15C>T 776 r.(=) p.(=) - intron 15
./. - c.776-15C>T 776 r.(=) p.(=) - intron 15
./. - c.776-15C>T 776 r.(=) p.(=) - intron 15
./. - c.776-15C>T 776 r.(=) p.(=) - intron 15
./. - c.776-15C>T 776 r.(=) p.(=) - intron 15
./. - c.776-15C>T 776 r.(=) p.(=) - intron 15
./. - c.776-15C>T 776 r.(=) p.(=) - intron 15
./. - c.776-15C>T 776 r.(=) p.(=) - intron 15
./. - c.1069-37T>C 1069 r.(=) p.(=) - intron 37
./. - c.1069-9T>C 1069 r.(=) p.(=) - intron 9
./. - c.1164G>A 1164 r.(?) p.(=) - coding-synonymous -
./. - c.1164G>A 1164 r.(?) p.(=) - coding-synonymous -
./. - c.1402C>G 1402 r.(?) p.(Leu468Val) - missense -
./. - c.1437C>T 1437 r.(?) p.(=) - coding-synonymous -
./. - c.1437C>T 1437 r.(?) p.(=) - coding-synonymous -
./. - c.1437C>T 1437 r.(?) p.(=) - coding-synonymous -
./. - c.1437C>T 1437 r.(?) p.(=) - coding-synonymous -
./. - c.1437C>T 1437 r.(?) p.(=) - coding-synonymous -
./. - c.1437C>T 1437 r.(?) p.(=) - coding-synonymous -
./. - c.1437C>T 1437 r.(?) p.(=) - coding-synonymous -
./. - c.1437C>T 1437 r.(?) p.(=) - coding-synonymous -
./. - c.1437C>T 1437 r.(?) p.(=) - coding-synonymous -
./. - c.1437C>T 1437 r.(?) p.(=) - coding-synonymous -
./. - c.1437C>T 1437 r.(?) p.(=) - coding-synonymous -
./. - c.1437C>T 1437 r.(?) p.(=) - coding-synonymous -
./. - c.1437C>T 1437 r.(?) p.(=) - coding-synonymous -
./. - c.1437C>T 1437 r.(?) p.(=) - coding-synonymous -
./. - c.1437C>T 1437 r.(?) p.(=) - coding-synonymous -
./. - c.1437C>T 1437 r.(?) p.(=) - coding-synonymous -
./. - c.1437C>T 1437 r.(?) p.(=) - coding-synonymous -
./. - c.1437C>T 1437 r.(?) p.(=) - coding-synonymous -
./. - c.1437C>T 1437 r.(?) p.(=) - coding-synonymous -
./. - c.1437C>T 1437 r.(?) p.(=) - coding-synonymous -
./. - c.1437C>T 1437 r.(?) p.(=) - coding-synonymous -
./. - c.1556G>A 1556 r.(?) p.(Gly519Glu) - missense -
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