Transcript #00022704 (NM_016628.4, WAC gene)

Transcript name transcript variant 1
Gene name WAC (WW domain containing adaptor with coiled-coil)
Chromosome 10
Transcript - NCBI ID NM_016628.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_057712.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

83 entries on 1 page. Showing entries 1 - 83.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.42-3C>A r.spl? p.?
-?/. - c.79-226T>G r.(=) p.(=)
+/. - c.112del r.(?) p.(Ser38Alafs*154)
+/. 3 c.139C>T r.(?) p.(Arg47*)
+/. 1 c.139C>T r.(?) p.(Arg47*)
+?/. - c.139C>T r.(?) p.(Arg47Ter)
./. - c.139C>T r.(?) p.(Arg47*)
-?/. - c.140G>A r.(?) p.(Arg47Gln)
?/. - c.144C>A r.(?) p.(Asp48Glu)
-?/. - c.149G>C r.(?) p.(Gly50Ala)
-?/. - c.192T>C r.(?) p.(Ser64=)
?/. - c.206A>G r.(?) p.(Tyr69Cys)
+?/. - c.263dup r.(?) p.(Arg89Glufs*21)
+?/. - c.263_266del r.(?) p.(Glu88Glyfs*103)
+/. - c.267_268dup r.(?) p.(Asp90Glyfs*103)
+?/. - c.272del r.(?) p.(Gly91Valfs*101)
+?/. - c.272del r.(?) p.(Gly91Valfs*101)
-?/. - c.275-23074T>C r.(=) p.(=)
-?/. - c.275-4dup r.spl? p.?
-?/. - c.275-4T>G r.spl? p.?
+?/. - c.292_293del r.(?) p.(Gln98ArgfsTer11)
?/. 4 c.307_309del r.(?) p.(Asn103del)
+/. 4 c.329C>A r.(?) p.(Ser110*)
+?/. - c.329C>A r.(?) p.(Ser110Ter)
+/. 8 c.356dup r.(?) p.(Asn119Lysfs*2)
?/. - c.356dup r.(?) p.(Asn119LysfsTer2)
+/. - c.374C>A r.(?) p.(Ser125*)
+/. 4 c.374C>A r.(?) p.(Ser125*)
+?/. - c.374C>A r.(?) p.(Ser125*)
?/. - c.377A>C r.(?) p.(Asp126Ala)
+/. 4i c.381+2T>C r.275_381del p.Gly92Alafs*3
+/. - c.381+4_381+7del r.spl? p.?
+/. _5_14 c.382-?_1944+?del r.? p.?
+/. - c.401_405del r.(?) p.(Asp134Valfs*2)
+/. 5 c.451C>T r.(?) p.(Arg151*)
+?/. - c.470G>A r.(?) p.(Trp157*)
+/. - c.482_483del r.(?) p.(Lys161Argfs*4)
+?/. - c.497+1G>A r.(?) p.(?)
+/. - c.498-2A>G r.spl p.?
-?/. - c.515A>C r.(?) p.(Glu172Ala)
+/. - c.523_524del r.(?) p.(Lys175Aspfs*10)
-?/. - c.539G>A r.(?) p.(Ser180Asn)
+/. - c.563_564insCC r.(?) p.(Arg188SerfsTer5)
-?/. - c.611-4A>T r.spl? p.?
?/. - c.709G>T r.(?) p.(Ala237Ser)
-?/. - c.721A>G r.(?) p.(Ser241Gly)
+?/. - c.748del r.(?) p.(Ile250Serfs*81)
+?/. - c.756del r.(?) p.(Val253Trpfs*78)
-?/. - c.769A>G r.(?) p.(Thr257Ala)
?/. - c.794C>G r.(?) p.(Ser265Cys)
-?/. - c.820C>A r.(?) p.(His274Asn)
+/. - c.851_866dup r.(?) p.(Lys290SerfsTer80)
+/. - c.914_917del r.(?) p.(Arg305Lysfs*25)
-?/. - c.929C>T r.(?) p.(Ser310Leu)
+/. - c.1007del r.(?) p.(Pro336Leufs*51)
+?/. - c.1052C>A r.(?) p.(Ser351Ter)
-?/. - c.1081A>C r.(?) p.(Asn361His)
+/. - c.1209_1212del r.(?) p.(His404Serfs*12)
?/. - c.1231_1233del r.(?) p.(Pro411del)
-?/. - c.1251G>A r.(?) p.(Thr417=)
+?/. - c.1285C>T r.(?) p.(Gln429Ter)
-?/. - c.1290C>G r.(?) p.(Ala430=)
+/. - c.1340del r.(?) p.(Pro447GlnfsTer9)
+/. - c.1346C>G r.(?) p.(Ser449*)
+/. - c.1358dup r.(?) p.(Arg454LysfsTer8)
+/. - c.1415del r.(?) p.(Pro472Leufs*13)
+?/. - c.1471_1472dup r.(?) p.(Gln492HisfsTer9)
+/. - c.1477_1480del r.(?) p.(Ser493ProfsTer6)
+/. - c.1537C>T r.(?) p.(Arg513Ter)
+/. - c.1537C>T r.(?) p.(Arg513Ter)
+/. - c.1648C>T r.(?) p.(Arg550*)
+/. - c.1648C>T r.(?) p.(Arg550*)
+/. - c.1648C>T r.(?) p.(Arg550Ter)
+/. 12 c.1661_1664del r.(?) p.(Ser554*)
+/. - c.1721G>A r.(?) p.(Trp574*)
+/. - c.1721G>A r.(?) p.(Trp574*)
+/. - c.1757T>G r.(?) p.(Leu586Ter)
?/. - c.1792A>G r.(?) p.(Met598Val)
+/. - c.1823dup r.(?) p.(Leu608PhefsTer9)
+/. - c.1852C>T r.(?) p.(Gln618*)
+/. - c.1852C>T r.(?) p.(Gln618Ter)
+?/. 13 c.1885_1886del r.(?) p.(Leu629Glufs*5)
?/. - c.1894_1896del r.(?) p.(Gln632del)
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