Transcript #00019356 (NM_015272.2, RPGRIP1L gene)

Transcript name Manually created transcript.
Gene name RPGRIP1L (RPGRIP1-like)
Chromosome 16
Transcript - NCBI ID NM_015272.2
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

58 entries on 1 page. Showing entries 1 - 58.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

Position     

RNA change     

Protein     

PolyPhen prediction     

GVS function     

Splice distance     
./. - c.-459T>C -459 r.(=) p.(=) - utr-5 -
./. - c.-407A>G -407 r.(=) p.(=) - utr-5 -
./. - c.530-29G>A 530 r.(=) p.(=) - intron 29
./. - c.530-29G>A 530 r.(=) p.(=) - intron 29
./. - c.530-29G>A 530 r.(=) p.(=) - intron 29
./. - c.530-29G>A 530 r.(=) p.(=) - intron 29
./. - c.530-29G>A 530 r.(=) p.(=) - intron 29
./. - c.530-29G>A 530 r.(=) p.(=) - intron 29
./. - c.530-29G>A 530 r.(=) p.(=) - intron 29
./. - c.685G>A 685 r.(?) p.(Ala229Thr) - missense -
./. - c.685G>A 685 r.(?) p.(Ala229Thr) - missense -
./. - c.883-50A>C 883 r.(=) p.(=) - intron 50
./. - c.1030-50A>C 1030 r.(=) p.(=) - intron 50
./. - c.1341G>A 1341 r.(?) p.(=) - coding-synonymous -
./. - c.1341G>A 1341 r.(?) p.(=) - coding-synonymous -
./. - c.2231G>A 2231 r.(?) p.(Arg744Gln) - missense -
./. - c.2684-40C>T 2684 r.(=) p.(=) - intron 40
./. - c.2684-40C>T 2684 r.(=) p.(=) - intron 40
./. - c.2959-32G>A 2959 r.(=) p.(=) - intron 32
./. - c.2959-32G>A 2959 r.(=) p.(=) - intron 32
./. - c.2959-32G>A 2959 r.(=) p.(=) - intron 32
./. - c.2959-32G>A 2959 r.(=) p.(=) - intron 32
./. - c.2959-32G>A 2959 r.(=) p.(=) - intron 32
./. - c.2959-32G>A 2959 r.(=) p.(=) - intron 32
./. - c.2959-32G>A 2959 r.(=) p.(=) - intron 32
./. - c.2959-32G>A 2959 r.(=) p.(=) - intron 32
./. - c.2959-32G>A 2959 r.(=) p.(=) - intron 32
./. - c.2959-32G>A 2959 r.(=) p.(=) - intron 32
./. - c.2959-32G>A 2959 r.(=) p.(=) - intron 32
./. - c.2959-32G>A 2959 r.(=) p.(=) - intron 32
./. - c.2959-32G>A 2959 r.(=) p.(=) - intron 32
./. - c.2959-32G>A 2959 r.(=) p.(=) - intron 32
./. - c.2959-32G>A 2959 r.(=) p.(=) - intron 32
./. - c.2959-32G>A 2959 r.(=) p.(=) - intron 32
./. - c.2959-32G>A 2959 r.(=) p.(=) - intron 32
./. - c.2959-32G>A 2959 r.(=) p.(=) - intron 32
./. - c.2959-32G>A 2959 r.(=) p.(=) - intron 32
./. - c.2959-32G>A 2959 r.(=) p.(=) - intron 32
./. - c.2959-32G>A 2959 r.(=) p.(=) - intron 32
./. - c.2959-15T>C 2959 r.(=) p.(=) - intron 15
./. - c.3073G>A 3073 r.(?) p.(Gly1025Ser) - missense -
./. - c.3073G>A 3073 r.(?) p.(Gly1025Ser) - missense -
./. - c.3073G>A 3073 r.(?) p.(Gly1025Ser) - missense -
./. - c.3073G>A 3073 r.(?) p.(Gly1025Ser) - missense -
./. - c.3073G>A 3073 r.(?) p.(Gly1025Ser) - missense -
./. - c.3073G>A 3073 r.(?) p.(Gly1025Ser) - missense -
./. - c.3073G>A 3073 r.(?) p.(Gly1025Ser) - missense -
./. - c.3790G>A 3790 r.(?) p.(Asp1264Asn) - missense -
./. - c.3790G>A 3790 r.(?) p.(Asp1264Asn) - missense -
./. - c.3790G>A 3790 r.(?) p.(Asp1264Asn) - missense -
./. - c.3790G>A 3790 r.(?) p.(Asp1264Asn) - missense -
./. - c.3790G>A 3790 r.(?) p.(Asp1264Asn) - missense -
./. - c.3790G>A 3790 r.(?) p.(Asp1264Asn) - missense -
./. - c.3936C>T 3936 r.(?) p.(=) - coding-synonymous -
./. - c.3936C>T 3936 r.(?) p.(=) - coding-synonymous -
./. - c.3936C>T 3936 r.(?) p.(=) - coding-synonymous -
./. - c.3936C>T 3936 r.(?) p.(=) - coding-synonymous -
./. - c.3936C>T 3936 r.(?) p.(=) - coding-synonymous -
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