Transcript #00009256 (NM_001166136.1, EVC2 gene)

Transcript name transcript variant 2
Gene name EVC2 (Ellis van Creveld syndrome 2)
Chromosome 4
Transcript - NCBI ID NM_001166136.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001159608.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2014-01-21 10:29:14 +01:00 (CET)
Date last edited N/A


Variants

197 entries on 2 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

Position     

RNA change     

Protein     

PolyPhen prediction     

GVS function     

Splice distance     
./. - c.-2769C>G -2769 r.(=) p.(=) - utr-5 -
./. - c.-2769C>G -2769 r.(=) p.(=) - utr-5 -
./. - c.-2769C>G -2769 r.(=) p.(=) - utr-5 -
./. - c.-2769C>G -2769 r.(=) p.(=) - utr-5 -
./. - c.-2769C>G -2769 r.(=) p.(=) - utr-5 -
./. - c.-2769C>G -2769 r.(=) p.(=) - utr-5 -
./. - c.-2769C>G -2769 r.(=) p.(=) - utr-5 -
./. - c.-2769C>G -2769 r.(=) p.(=) - utr-5 -
./. - c.-13+301G>A -13 r.(=) p.(=) - intron 301
./. - c.-13+301G>A -13 r.(=) p.(=) - intron 301
./. - c.-13+301G>A -13 r.(=) p.(=) - intron 301
./. - c.-13+301G>A -13 r.(=) p.(=) - intron 301
./. - c.-13+301G>A -13 r.(=) p.(=) - intron 301
./. - c.-13+301G>A -13 r.(=) p.(=) - intron 301
./. - c.-13+301G>A -13 r.(=) p.(=) - intron 301
./. - c.-13+301G>A -13 r.(=) p.(=) - intron 301
./. - c.-13+367C>T -13 r.(=) p.(=) - intron 367
./. - c.-13+367C>T -13 r.(=) p.(=) - intron 367
./. - c.-13+367C>T -13 r.(=) p.(=) - intron 367
./. - c.-13+367C>T -13 r.(=) p.(=) - intron 367
./. - c.-13+367C>T -13 r.(=) p.(=) - intron 367
./. - c.-13+367C>T -13 r.(=) p.(=) - intron 367
./. - c.-13+367C>T -13 r.(=) p.(=) - intron 367
./. - c.-13+367C>T -13 r.(=) p.(=) - intron 367
./. - c.-13+367C>T -13 r.(=) p.(=) - intron 367
./. - c.-13+367C>T -13 r.(=) p.(=) - intron 367
./. - c.-13+367C>T -13 r.(=) p.(=) - intron 367
./. - c.44-36C>T 44 r.(=) p.(=) - intron 36
./. - c.44-36C>T 44 r.(=) p.(=) - intron 36
./. - c.44-36C>T 44 r.(=) p.(=) - intron 36
./. - c.44-36C>T 44 r.(=) p.(=) - intron 36
./. - c.44-36C>T 44 r.(=) p.(=) - intron 36
./. - c.44-36C>T 44 r.(=) p.(=) - intron 36
./. - c.44-36C>T 44 r.(=) p.(=) - intron 36
./. - c.67T>C 67 r.(?) p.(=) - coding-synonymous -
./. - c.210+31A>G 210 r.(=) p.(=) - intron 31
./. - c.279+15G>A 279 r.(=) p.(=) - intron 15
./. - c.279+15G>A 279 r.(=) p.(=) - intron 15
./. - c.279+15G>A 279 r.(=) p.(=) - intron 15
./. - c.279+15G>A 279 r.(=) p.(=) - intron 15
./. - c.279+15G>A 279 r.(=) p.(=) - intron 15
./. - c.313A>G 313 r.(?) p.(Ile105Val) - missense -
./. - c.313A>G 313 r.(?) p.(Ile105Val) - missense -
./. - c.313A>G 313 r.(?) p.(Ile105Val) - missense -
./. - c.448A>G 448 r.(?) p.(Ser150Gly) - missense -
./. - c.448A>G 448 r.(?) p.(Ser150Gly) - missense -
./. - c.448A>G 448 r.(?) p.(Ser150Gly) - missense -
./. - c.448A>G 448 r.(?) p.(Ser150Gly) - missense -
./. - c.448A>G 448 r.(?) p.(Ser150Gly) - missense -
./. - c.448A>G 448 r.(?) p.(Ser150Gly) - missense -
./. - c.574C>T 574 r.(?) p.(Arg192Trp) - missense-near-splice -
./. - c.577-43C>G 577 r.(=) p.(=) - intron 43
./. - c.577-43C>G 577 r.(=) p.(=) - intron 43
./. - c.624C>T 624 r.(?) p.(=) - coding-synonymous -
./. - c.905+34_905+35del 905 r.(=) p.(=) - intron 34
./. - c.905+34_905+35del 905 r.(=) p.(=) - intron 34
./. - c.906-47G>C 906 r.(=) p.(=) - intron 47
./. - c.906-47G>C 906 r.(=) p.(=) - intron 47
./. - c.906-47G>C 906 r.(=) p.(=) - intron 47
./. - c.906-47G>C 906 r.(=) p.(=) - intron 47
./. - c.906-47G>C 906 r.(=) p.(=) - intron 47
./. - c.906-47G>C 906 r.(=) p.(=) - intron 47
./. - c.906-11G>A 906 r.(=) p.(=) - intron 11
./. - c.906-11G>A 906 r.(=) p.(=) - intron 11
./. - c.906-11G>A 906 r.(=) p.(=) - intron 11
./. - c.968G>A 968 r.(?) p.(Ser323Asn) - missense -
./. - c.968G>A 968 r.(?) p.(Ser323Asn) - missense -
./. - c.968G>A 968 r.(?) p.(Ser323Asn) - missense -
./. - c.968G>A 968 r.(?) p.(Ser323Asn) - missense -
./. - c.968G>A 968 r.(?) p.(Ser323Asn) - missense -
./. - c.968G>A 968 r.(?) p.(Ser323Asn) - missense -
./. - c.1101C>T 1101 r.(?) p.(=) - coding-synonymous -
./. - c.1197A>G 1197 r.(?) p.(=) - coding-synonymous -
./. - c.1197A>G 1197 r.(?) p.(=) - coding-synonymous -
./. - c.1197A>G 1197 r.(?) p.(=) - coding-synonymous -
./. - c.1197A>G 1197 r.(?) p.(=) - coding-synonymous -
./. - c.1197A>G 1197 r.(?) p.(=) - coding-synonymous -
./. - c.1197A>G 1197 r.(?) p.(=) - coding-synonymous -
./. - c.1197A>G 1197 r.(?) p.(=) - coding-synonymous -
./. - c.1197A>G 1197 r.(?) p.(=) - coding-synonymous -
./. - c.1197A>G 1197 r.(?) p.(=) - coding-synonymous -
./. - c.1197A>G 1197 r.(?) p.(=) - coding-synonymous -
./. - c.1197A>G 1197 r.(?) p.(=) - coding-synonymous -
./. - c.1197A>G 1197 r.(?) p.(=) - coding-synonymous -
./. - c.1197A>G 1197 r.(?) p.(=) - coding-synonymous -
./. - c.1197A>G 1197 r.(?) p.(=) - coding-synonymous -
./. - c.1197A>G 1197 r.(?) p.(=) - coding-synonymous -
./. - c.1231-7T>C 1231 r.(=) p.(=) - splice 7
./. - c.1471-20T>G 1471 r.(=) p.(=) - intron 20
./. - c.1471-20T>G 1471 r.(=) p.(=) - intron 20
./. - c.1471-20T>G 1471 r.(=) p.(=) - intron 20
./. - c.1471-20T>G 1471 r.(=) p.(=) - intron 20
./. - c.1646+29G>A 1646 r.(=) p.(=) - intron 29
./. - c.1646+29G>A 1646 r.(=) p.(=) - intron 29
./. - c.1646+29G>A 1646 r.(=) p.(=) - intron 29
./. - c.1646+29G>A 1646 r.(=) p.(=) - intron 29
./. - c.1646+29G>A 1646 r.(=) p.(=) - intron 29
./. - c.1646+29G>A 1646 r.(=) p.(=) - intron 29
./. - c.1648G>A 1648 r.(?) p.(Ala550Thr) - missense-near-splice -
./. - c.1806+5A>G 1806 r.spl? p.? - splice 5
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