Transcript #00008757 (NM_023034.1, WHSC1L1 gene)

Transcript name transcript variant long
Gene name WHSC1L1 (Wolf-Hirschhorn syndrome candidate 1-like 1)
Chromosome 8
Transcript - NCBI ID NM_023034.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_075447.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2013-10-30 15:39:55 +01:00 (CET)
Date last edited N/A


Variants

21 entries on 1 page. Showing entries 1 - 21.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

Position     

RNA change     

Protein     

PolyPhen prediction     

GVS function     

Splice distance     
./. - c.1148G>C 1148 r.(?) p.(Arg383Pro) - missense -
./. - c.1833A>C 1833 r.(?) p.(=) - coding-synonymous -
./. - c.2116-43G>A 2116 r.(=) p.(=) - intron 43
./. - c.3105G>A 3105 r.(?) p.(=) - coding-synonymous -
./. - c.3636C>T 3636 r.(?) p.(=) - coding-synonymous -
./. - c.3760+3A>G 3760 r.spl? p.? - splice 3
./. - c.3760+3A>G 3760 r.spl? p.? - splice 3
./. - c.3760+3A>G 3760 r.spl? p.? - splice 3
./. - c.4072+21C>T 4072 r.(=) p.(=) - intron 21
./. - c.4072+21C>T 4072 r.(=) p.(=) - intron 21
./. - c.4072+21C>T 4072 r.(=) p.(=) - intron 21
./. - c.4072+21C>T 4072 r.(=) p.(=) - intron 21
./. - c.4072+21C>T 4072 r.(=) p.(=) - intron 21
./. - c.4072+21C>T 4072 r.(=) p.(=) - intron 21
./. - c.4072+21C>T 4072 r.(=) p.(=) - intron 21
./. - c.4072+21C>T 4072 r.(=) p.(=) - intron 21
./. - c.4072+21C>T 4072 r.(=) p.(=) - intron 21
./. - c.4072+21C>T 4072 r.(=) p.(=) - intron 21
./. - c.4072+21C>T 4072 r.(=) p.(=) - intron 21
./. - c.4072+21C>T 4072 r.(=) p.(=) - intron 21
./. - c.4072+21C>T 4072 r.(=) p.(=) - intron 21
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