Transcript #00019464 (NM_005631.4, SMO gene)

Transcript name smoothened, frizzled family receptor
Gene name SMO (smoothened, frizzled family receptor)
Chromosome 7
Transcript - NCBI ID NM_005631.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_005622.1
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

71 entries on 1 page. Showing entries 1 - 71.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
./. - c.-7828929_*6721667del r.0? p.0?
+?/. - c.-50670_332-2504del r.0? p.0?
?/. - c.64_69dup r.(?) p.(Leu22_Leu23dup)
?/. - c.64_69dup r.(?) p.(Leu22_Leu23dup)
?/. - c.67_69del r.(?) p.(Leu23del)
?/. - c.115_138del r.(?) p.(Pro39_Gly46del)
-?/. - c.125G>A r.(?) p.(Arg42Gln)
-?/. - c.160G>A r.(?) p.(Val54Met)
?/. - c.160G>A r.(?) p.(Val54Met)
?/. - c.280G>A r.(?) p.(Gly94Arg)
?/. - c.287C>A r.(?) p.(Ser96*)
?/. - c.385G>A r.(?) p.(Val129Ile)
?/. - c.412C>T r.(?) p.(Arg138Trp)
?/. - c.481C>T r.(?) p.(Arg161Trp)
?/. - c.485G>T r.(?) p.(Gly162Val)
+?/. - c.502C>G r.(?) p.(Arg168Gly)
?/. - c.503G>A r.(?) p.(Arg168His)
?/. - c.503G>A r.(?) p.(Arg168His)
?/. - c.517C>T r.(?) p.(Arg173Cys)
+/. - c.562_565del r.(?) p.(Asn188Valfs*113)
+/. - c.567_570del r.(?) p.(Ser189Argfs*112)
-?/. - c.735G>A r.(?) p.(Thr245=)
+?/. - c.781C>T r.(?) p.(Arg261Cys)
-?/. - c.808G>A r.(?) p.(Val270Ile)
-?/. - c.819C>T r.(?) p.(Cys273=)
?/. - c.828G>A r.(?) p.(=)
+?/. - c.1199G>A r.(1199g>a) p.(Arg400His)
+?/. - c.1199G>A r.(1199g>a) p.(Arg400His)
+?/. - c.1199G>A r.(1199g>a) p.(Arg400His)
-?/. - c.1203G>C r.(?) p.(Ala401=)
+/. 6 c.1234C>T r.(?) p.(Leu412Phe)
+/. 6 c.1234C>T r.(?) p.(Leu412Phe)
+/. 6 c.1234C>T r.(?) p.(Leu412Phe)
+/. 6 c.1234C>T r.(?) p.(Leu412Phe)
+/. 6 c.1234C>T r.(?) p.(Leu412Phe)
+/. 6 c.1234C>T r.(?) p.(Leu412Phe)
+/. 6 c.1234C>T r.(?) p.(Leu412Phe)
+/. 6 c.1234C>T r.(?) p.(Leu412Phe)
+/. - c.1234C>T r.(?) p.(Leu412Phe)
?/. - c.1252T>C r.(?) p.(Phe418Leu)
+?/. - c.1276_1277del r.(?) p.(Leu426Valfs*13)
+?/. - c.1276_1277del r.(?) p.(Leu426ValfsTer13)
+?/. - c.1285A>T r.[1285a>u,1265_1290del] p.[Ile429Phe,Gly422Glufs∗9]
+?/. - c.1339G>T r.(?) p.(Glu447*)
+/. - c.1416C>T r.[1416C>U, 1358_1466del] p.[Tyr472Tyr, Gly453AspfsTer6]
+/. - c.1416C>T r.[1416c>u,1358_1466del] p.[Tyr472Tyr,Gly453AspfsTer6]
+/. - c.1416C>T r.[1416c>u,1358_1466del] p.[Tyr472Tyr,Gly453AspfsTer6]
+?/. - c.1453C>G r.(?) p.(Arg485Gly)
+/. - c.1611G>A r.(?) p.(Trp537*)
?/. - c.1684C>T r.(?) p.(Arg562Trp)
+/. - c.1685G>A r.(?) p.(Arg562Gln)
+/. - c.1685G>A r.(?) p.(Arg562Gln)
+?/. - c.1726C>T r.(?) p.(Arg576Trp)
+?/. - c.1726C>T r.(?) p.(Arg576Trp)
+?/. - c.1726C>T r.(?) p.(Arg576Trp)
+?/. - c.1727G>A r.(?) p.(Arg576Gln)
-?/. - c.1731C>T r.(?) p.(=)
?/. - c.1882C>T r.(?) p.(Arg628Trp)
-?/. - c.1921C>G r.(?) p.(Pro641Ala)
?/. - c.1921C>G r.(?) p.(Pro641Ala)
-?/. - c.1939C>T r.(?) p.(Pro647Ser)
?/. - c.2002C>T r.(?) p.(Arg668Cys)
?/. - c.2093C>G r.(?) p.(Pro698Arg)
?/. - c.2093C>G r.(?) p.(Pro698Arg)
?/. - c.2096G>A r.(?) p.(Ser699Asn)
-?/. - c.2147C>A r.(?) p.(Ala716Glu)
?/. - c.2177G>A r.(?) p.(Arg726Gln)
-?/. - c.2255C>T r.(?) p.(Ala752Val)
-?/. - c.2265C>T r.(?) p.(Pro755=)
+?/. - c.2291_2292del r.2291_2292del p.Gln764Argfs*52
?/. - c.2314C>T r.(?) p.(Arg772Cys)
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