Transcript #00011892 (NM_020166.3, MCCC1 gene)

Transcript name methylcrotonoyl-CoA carboxylase 1 (alpha)
Gene name MCCC1 (methylcrotonoyl-CoA carboxylase 1 (alpha))
Chromosome 3
Transcript - NCBI ID NM_020166.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_064551.3
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

79 entries on 1 page. Showing entries 1 - 79.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+?/. - c.? r.? p.?
?/. - c.130G>T r.(?) p.(Ala44Ser)
?/. - c.131C>T r.(?) p.(Ala44Val)
?/. - c.131C>T r.(?) p.(Ala44Val)
+/. - c.137-2A>G r.spl p.?
+?/. - c.137-2A>G r.spl p.?
+?/. - c.137-2A>G r.spl? p.?
+/. - c.137-2A>G r.spl? p.?
?/. - c.172G>A r.(?) p.(Gly58Arg)
?/. - c.181G>T r.(?) p.(Ala61Ser)
?/. - c.184T>G r.(?) p.(Cys62Gly)
?/. - c.190G>A r.(?) p.(Val64Met)
?/. - c.230C>T r.(?) p.(Ala77Val)
?/. - c.295G>A r.(?) p.(Gly99Ser)
+/. - c.310C>T r.(?) p.(Gln104Ter)
+/. - c.369+1G>A r.(?) p.?
+?/. - c.369+1G>A r.spl p.?
+?/. - c.388G>A r.(?) p.(Gly130Ser)
?/. - c.388G>A r.(?) p.(Gly130Ser)
?/. - c.388G>A r.(?) p.(Gly130Ser)
-/. - c.396C>T r.(?) p.(Leu132=)
-/. - c.396C>T r.(?) p.(Leu132=)
?/. - c.416C>T r.(?) p.(Ala139Val)
?/. - c.490del r.(?) p.(Ser164AlafsTer6)
+?/. - c.539G>T r.(?) p.(Gly180Val)
+?/. - c.559T>C r.(?) p.(Ser187Pro)
+/. - c.639+2T>A r.spl p.(Ser164Argfs*3)
+/. - c.684dup r.(?) p.(Glu229Argfs*8)
+/. 7 c.684dup r.(?) p.(Glu229ArgfsTer8)
+?/. - c.694C>T r.(?) p.(Arg232Trp)
?/. - c.785G>A r.(?) p.(Gly262Asp)
+/. - c.841C>T r.(?) p.(Arg281Ter)
?/. - c.863A>G r.(?) p.(Glu288Gly)
+?/. - c.872C>T r.(?) p.(Ala291Val)
?/. - c.872C>T r.(?) p.(Ala291Val)
+?/. - c.872C>T r.(?) p.(Ala291Val)
+/. - c.872C>T r.(?) p.(Ala291Val)
+?/. - c.873G>A r.(?) p.(Ala291=)
+/. - c.945T>A r.(?) p.(Tyr315*)
+?/. - c.1008G>C r.(?) p.(Met336Ile)
+?/. 10 c.1008G>C r.(?) p.(Met336Ile)
+/. - c.1013_1015del r.(?) p.(Thr338del)
?/. - c.1046T>C r.(?) p.(Met349Thr)
+?/. - c.1069G>T r.(?) p.(Glu357Ter)
+/. - c.1114C>T r.(?) p.(Gln372Ter)
?/. - c.1136G>A r.(?) p.(Gly379Asp)
+?/. - c.1147G>A r.(?) p.(Glu383Lys)
+/. - c.1155A>C r.(?) p.(Arg385Ser)
+?/. - c.1155A>C r.(?) p.(Arg385Ser)
+?/. - c.1155A>C r.(?) p.(Arg385Ser)
+?/. - c.1155A>C r.(?) p.(Arg385Ser)
+/. - c.1193_1194del r.(?) p.(Val398Glyfs*19)
+/. - c.1193_1194del r.(?) p.(Val398Glyfs*19)
+?/. - c.1261C>T r.(?) p.(Arg421Trp)
+?/. 11 c.1261C>T r.(?) p.(Arg421Trp)
?/. - c.1302T>G r.(?) p.(Ile434Met)
+/. - c.1331G>A r.(?) p.(Arg444His)
+?/. - c.1331G>A r.(?) p.(Arg444His)
?/. - c.1358A>G r.(?) p.(Tyr453Cys)
?/. - c.1381G>T r.(?) p.(Val461Phe)
-/. - c.1391A>C r.(?) p.(His464Pro)
-/. - c.1391A>C r.(?) p.(His464Pro)
-/. - c.1391A>C r.(?) p.(His464Pro)
?/. - c.1456A>G r.(?) p.(Thr486Ala)
?/. - c.1492C>T r.(?) p.(Leu498Phe)
-?/. - c.1504G>C r.(?) p.(Ala502Pro)
+/. - c.1527C>A r.(?) p.(Cys509*)
+?/. - c.1594G>C r.(?) p.(Asp532His)
?/. - c.1614G>A r.(=) p.(=)
?/. - c.1619G>A r.(?) p.(Ser540Asn)
+/. - c.1679dup r.(?) p.(Asn560LysfsTer10)
-?/. - c.1795A>G r.(?) p.(Lys599Glu)
-?/. - c.1894C>T r.(?) p.(Pro632Ser)
?/. - c.2046G>C r.(?) p.(Met682Ile)
?/. - c.2085delinsAA r.(?) p.(Val697Serfs*19)
+?/. - c.2088dup r.(?) p.(Val697SerfsTer19)
+/. - c.2088dup r.(?) p.(Val697SerfsTer19)
-?/. - c.2149G>A r.(?) p.(Glu717Lys)
-?/. - c.2171C>T r.(?) p.(Ser724Leu)
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