Transcript #00016988 (NM_147127.4, EVC2 gene)

Transcript name Manually created transcript. (removed from reference sequence)
Gene name EVC2 (Ellis van Creveld syndrome 2)
Chromosome 4
Transcript - NCBI ID NM_147127.4
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

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.-3072C>G -3072 r.(=) p.(=) - utr-5 -
./. - c.-3072C>G -3072 r.(=) p.(=) - utr-5 -
./. - c.-3072C>G -3072 r.(=) p.(=) - utr-5 -
./. - c.-3072C>G -3072 r.(=) p.(=) - utr-5 -
./. - c.-3072C>G -3072 r.(=) p.(=) - utr-5 -
./. - c.-3072C>G -3072 r.(=) p.(=) - utr-5 -
./. - c.-3072C>G -3072 r.(=) p.(=) - utr-5 -
./. - c.-3072C>G -3072 r.(=) p.(=) - utr-5 -
./. - c.-15G>A -15 r.(=) p.(=) - utr-5 -
./. - c.-15G>A -15 r.(=) p.(=) - utr-5 -
./. - c.-15G>A -15 r.(=) p.(=) - utr-5 -
./. - c.-15G>A -15 r.(=) p.(=) - utr-5 -
./. - c.-15G>A -15 r.(=) p.(=) - utr-5 -
./. - c.-15G>A -15 r.(=) p.(=) - utr-5 -
./. - c.-15G>A -15 r.(=) p.(=) - utr-5 -
./. - c.-15G>A -15 r.(=) p.(=) - utr-5 -
./. - c.52C>T 52 r.(?) p.(Leu18Phe) - missense -
./. - c.52C>T 52 r.(?) p.(Leu18Phe) - missense -
./. - c.52C>T 52 r.(?) p.(Leu18Phe) - missense -
./. - c.52C>T 52 r.(?) p.(Leu18Phe) - missense -
./. - c.52C>T 52 r.(?) p.(Leu18Phe) - missense -
./. - c.52C>T 52 r.(?) p.(Leu18Phe) - missense -
./. - c.52C>T 52 r.(?) p.(Leu18Phe) - missense -
./. - c.52C>T 52 r.(?) p.(Leu18Phe) - missense -
./. - c.52C>T 52 r.(?) p.(Leu18Phe) - missense -
./. - c.52C>T 52 r.(?) p.(Leu18Phe) - missense -
./. - c.52C>T 52 r.(?) p.(Leu18Phe) - missense -
./. - c.284-36C>T 284 r.(=) p.(=) - intron 36
./. - c.284-36C>T 284 r.(=) p.(=) - intron 36
./. - c.284-36C>T 284 r.(=) p.(=) - intron 36
./. - c.284-36C>T 284 r.(=) p.(=) - intron 36
./. - c.284-36C>T 284 r.(=) p.(=) - intron 36
./. - c.284-36C>T 284 r.(=) p.(=) - intron 36
./. - c.284-36C>T 284 r.(=) p.(=) - intron 36
./. - c.307T>C 307 r.(?) p.(=) - coding-synonymous -
./. - c.450+31A>G 450 r.(=) p.(=) - intron 31
./. - c.519+15G>A 519 r.(=) p.(=) - intron 15
./. - c.519+15G>A 519 r.(=) p.(=) - intron 15
./. - c.519+15G>A 519 r.(=) p.(=) - intron 15
./. - c.519+15G>A 519 r.(=) p.(=) - intron 15
./. - c.519+15G>A 519 r.(=) p.(=) - intron 15
./. - c.553A>G 553 r.(?) p.(Ile185Val) - missense -
./. - c.553A>G 553 r.(?) p.(Ile185Val) - missense -
./. - c.553A>G 553 r.(?) p.(Ile185Val) - missense -
./. - c.688A>G 688 r.(?) p.(Ser230Gly) - missense -
./. - c.688A>G 688 r.(?) p.(Ser230Gly) - missense -
./. - c.688A>G 688 r.(?) p.(Ser230Gly) - missense -
./. - c.688A>G 688 r.(?) p.(Ser230Gly) - missense -
./. - c.688A>G 688 r.(?) p.(Ser230Gly) - missense -
./. - c.688A>G 688 r.(?) p.(Ser230Gly) - missense -
./. - c.814C>T 814 r.(?) p.(Arg272Trp) - missense-near-splice -
./. - c.817-43C>G 817 r.(=) p.(=) - intron 43
./. - c.817-43C>G 817 r.(=) p.(=) - intron 43
./. - c.864C>T 864 r.(?) p.(=) - coding-synonymous -
./. - c.1145+34_1145+35del 1145 r.(=) p.(=) - intron 34
./. - c.1145+34_1145+35del 1145 r.(=) p.(=) - intron 34
./. - c.1146-47G>C 1146 r.(=) p.(=) - intron 47
./. - c.1146-47G>C 1146 r.(=) p.(=) - intron 47
./. - c.1146-47G>C 1146 r.(=) p.(=) - intron 47
./. - c.1146-47G>C 1146 r.(=) p.(=) - intron 47
./. - c.1146-47G>C 1146 r.(=) p.(=) - intron 47
./. - c.1146-47G>C 1146 r.(=) p.(=) - intron 47
./. - c.1146-11G>A 1146 r.(=) p.(=) - intron 11
./. - c.1146-11G>A 1146 r.(=) p.(=) - intron 11
./. - c.1146-11G>A 1146 r.(=) p.(=) - intron 11
./. - c.1208G>A 1208 r.(?) p.(Ser403Asn) - missense -
./. - c.1208G>A 1208 r.(?) p.(Ser403Asn) - missense -
./. - c.1208G>A 1208 r.(?) p.(Ser403Asn) - missense -
./. - c.1208G>A 1208 r.(?) p.(Ser403Asn) - missense -
./. - c.1208G>A 1208 r.(?) p.(Ser403Asn) - missense -
./. - c.1208G>A 1208 r.(?) p.(Ser403Asn) - missense -
./. - c.1341C>T 1341 r.(?) p.(=) - coding-synonymous -
./. - c.1437A>G 1437 r.(?) p.(=) - coding-synonymous -
./. - c.1437A>G 1437 r.(?) p.(=) - coding-synonymous -
./. - c.1437A>G 1437 r.(?) p.(=) - coding-synonymous -
./. - c.1437A>G 1437 r.(?) p.(=) - coding-synonymous -
./. - c.1437A>G 1437 r.(?) p.(=) - coding-synonymous -
./. - c.1437A>G 1437 r.(?) p.(=) - coding-synonymous -
./. - c.1437A>G 1437 r.(?) p.(=) - coding-synonymous -
./. - c.1437A>G 1437 r.(?) p.(=) - coding-synonymous -
./. - c.1437A>G 1437 r.(?) p.(=) - coding-synonymous -
./. - c.1437A>G 1437 r.(?) p.(=) - coding-synonymous -
./. - c.1437A>G 1437 r.(?) p.(=) - coding-synonymous -
./. - c.1437A>G 1437 r.(?) p.(=) - coding-synonymous -
./. - c.1437A>G 1437 r.(?) p.(=) - coding-synonymous -
./. - c.1437A>G 1437 r.(?) p.(=) - coding-synonymous -
./. - c.1437A>G 1437 r.(?) p.(=) - coding-synonymous -
./. - c.1471-7T>C 1471 r.(=) p.(=) - splice 7
./. - c.1711-20T>G 1711 r.(=) p.(=) - intron 20
./. - c.1711-20T>G 1711 r.(=) p.(=) - intron 20
./. - c.1711-20T>G 1711 r.(=) p.(=) - intron 20
./. - c.1711-20T>G 1711 r.(=) p.(=) - intron 20
./. - c.1886+29G>A 1886 r.(=) p.(=) - intron 29
./. - c.1886+29G>A 1886 r.(=) p.(=) - intron 29
./. - c.1886+29G>A 1886 r.(=) p.(=) - intron 29
./. - c.1886+29G>A 1886 r.(=) p.(=) - intron 29
./. - c.1886+29G>A 1886 r.(=) p.(=) - intron 29
./. - c.1886+29G>A 1886 r.(=) p.(=) - intron 29
./. - c.1888G>A 1888 r.(?) p.(Ala630Thr) - missense-near-splice -
./. - c.2046+5A>G 2046 r.spl? p.? - splice 5
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