Transcript #00046233 (NM_001278690.1, FGFR1OP gene)

Transcript name transcript variant 3
Gene name FGFR1OP (FGFR1 oncogene partner)
Chromosome 6
Transcript - NCBI ID NM_001278690.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001265619.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2015-01-20 21:56:40 +01:00 (CET)
Date last edited N/A


Variants

72 entries on 1 page. Showing entries 1 - 72.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

Position     

RNA change     

Protein     

PolyPhen prediction     

GVS function     

Splice distance     
./. - c.13G>A 13 r.(?) p.(Ala5Thr) - missense -
./. - c.13G>A 13 r.(?) p.(Ala5Thr) - missense -
./. - c.13G>A 13 r.(?) p.(Ala5Thr) - missense -
./. - c.103-9T>C 103 r.(=) p.(=) - intron 9
./. - c.103-9T>C 103 r.(=) p.(=) - intron 9
./. - c.103-9T>C 103 r.(=) p.(=) - intron 9
./. - c.103-9T>C 103 r.(=) p.(=) - intron 9
./. - c.103-9T>C 103 r.(=) p.(=) - intron 9
./. - c.103-9T>C 103 r.(=) p.(=) - intron 9
./. - c.103-9T>C 103 r.(=) p.(=) - intron 9
./. - c.103-9T>C 103 r.(=) p.(=) - intron 9
./. - c.103-9T>C 103 r.(=) p.(=) - intron 9
./. - c.103-9T>C 103 r.(=) p.(=) - intron 9
./. - c.103-9T>C 103 r.(=) p.(=) - intron 9
./. - c.103-9T>C 103 r.(=) p.(=) - intron 9
./. - c.103-9T>C 103 r.(=) p.(=) - intron 9
./. - c.103-9T>C 103 r.(=) p.(=) - intron 9
./. - c.103-9T>C 103 r.(=) p.(=) - intron 9
./. - c.103-9T>C 103 r.(=) p.(=) - intron 9
./. - c.103-9T>C 103 r.(=) p.(=) - intron 9
./. - c.103-9T>C 103 r.(=) p.(=) - intron 9
./. - c.212-38G>A 212 r.(=) p.(=) - intron 38
./. - c.212-38G>A 212 r.(=) p.(=) - intron 38
./. - c.212-38G>A 212 r.(=) p.(=) - intron 38
./. - c.438+46G>A 438 r.(=) p.(=) - intron 46
./. - c.438+46G>A 438 r.(=) p.(=) - intron 46
./. - c.470C>T 470 r.(?) p.(Thr157Ile) - missense -
./. - c.470C>T 470 r.(?) p.(Thr157Ile) - missense -
./. - c.665+36T>C 665 r.(=) p.(=) - intron 36
./. - c.665+36T>C 665 r.(=) p.(=) - intron 36
./. - c.665+36T>C 665 r.(=) p.(=) - intron 36
./. - c.665+36T>C 665 r.(=) p.(=) - intron 36
./. - c.665+36T>C 665 r.(=) p.(=) - intron 36
./. - c.665+36T>C 665 r.(=) p.(=) - intron 36
./. - c.665+36T>C 665 r.(=) p.(=) - intron 36
./. - c.665+36T>C 665 r.(=) p.(=) - intron 36
./. - c.665+36T>C 665 r.(=) p.(=) - intron 36
./. - c.665+36T>C 665 r.(=) p.(=) - intron 36
./. - c.665+36T>C 665 r.(=) p.(=) - intron 36
./. - c.665+36T>C 665 r.(=) p.(=) - intron 36
./. - c.665+36T>C 665 r.(=) p.(=) - intron 36
./. - c.665+36T>C 665 r.(=) p.(=) - intron 36
./. - c.672G>T 672 r.(?) p.(Lys224Asn) - missense -
./. - c.672G>T 672 r.(?) p.(Lys224Asn) - missense -
./. - c.672G>T 672 r.(?) p.(Lys224Asn) - missense -
./. - c.688G>C 688 r.(?) p.(Ala230Pro) - missense -
./. - c.688G>C 688 r.(?) p.(Ala230Pro) - missense -
./. - c.688G>C 688 r.(?) p.(Ala230Pro) - missense -
./. - c.688G>C 688 r.(?) p.(Ala230Pro) - missense -
./. - c.778+16T>C 778 r.(=) p.(=) - intron 16
./. - c.778+16T>C 778 r.(=) p.(=) - intron 16
./. - c.778+16T>C 778 r.(=) p.(=) - intron 16
./. - c.778+16T>C 778 r.(=) p.(=) - intron 16
./. - c.847+25C>T 847 r.(=) p.(=) - intron 25
./. - c.847+25C>T 847 r.(=) p.(=) - intron 25
./. - c.847+25C>T 847 r.(=) p.(=) - intron 25
./. - c.847+25C>T 847 r.(=) p.(=) - intron 25
./. - c.847+25C>T 847 r.(=) p.(=) - intron 25
./. - c.847+25C>T 847 r.(=) p.(=) - intron 25
./. - c.847+25C>T 847 r.(=) p.(=) - intron 25
./. - c.847+25C>T 847 r.(=) p.(=) - intron 25
./. - c.847+25C>T 847 r.(=) p.(=) - intron 25
./. - c.847+25C>T 847 r.(=) p.(=) - intron 25
./. - c.847+25C>T 847 r.(=) p.(=) - intron 25
./. - c.847+25C>T 847 r.(=) p.(=) - intron 25
./. - c.847+25C>T 847 r.(=) p.(=) - intron 25
./. - c.847+25C>T 847 r.(=) p.(=) - intron 25
./. - c.847+25C>T 847 r.(=) p.(=) - intron 25
./. - c.847+25C>T 847 r.(=) p.(=) - intron 25
./. - c.847+25C>T 847 r.(=) p.(=) - intron 25
./. - c.847+25C>T 847 r.(=) p.(=) - intron 25
./. - c.847+25C>T 847 r.(=) p.(=) - intron 25
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