Transcript #00013702 (NM_052845.3, MMAB gene)

Transcript name transcript variant 1
Gene name MMAB (methylmalonic aciduria (cobalamin deficiency) cblB type)
Chromosome 12
Transcript - NCBI ID NM_052845.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_443077.1
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

87 entries on 1 page. Showing entries 1 - 87.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.-2672C>A r.(?) p.(=)
+/. - c.-2664_-2517del r.(?) p.(=)
-?/. - c.-2655T>C r.(?) p.(=)
-?/. - c.-2655T>C r.(?) p.(=)
?/. - c.-2644A>T r.(?) p.(=)
+/. - c.-2625C>T r.(?) p.(=)
+/. - c.-2624C>T r.(?) p.(=)
+/. - c.-2624C>T r.(?) p.(=)
+/. - c.-2624C>T r.(?) p.(=)
+/. - c.-2624C>T r.(?) p.(=)
-?/. - c.-2605T>C r.(?) p.(=)
-/. - c.-2594C>T r.(?) p.(=)
-/. - c.-2594C>T r.(?) p.(=)
+?/. - c.-2590G>A r.(?) p.(=)
+/. - c.-2567_-2566del r.(?) p.(=)
?/. - c.-2561A>G r.(?) p.(=)
?/. - c.-2558C>A r.(?) p.(=)
?/. - c.-2558C>T r.(?) p.(=)
+?/. - c.-2557G>A r.(?) p.(=)
+/. - c.-2555A>G r.(?) p.(=)
+?/. - c.-2546C>G r.(?) p.(=)
-?/. - c.-2544C>T r.(?) p.(=)
+/. - c.-2543A>G r.(?) p.(=)
+/. - c.-2525del r.(?) p.(=)
+/. - c.-2521C>T r.(?) p.(=)
-?/. - c.-2456C>T r.(?) p.(=)
-?/. - c.-1597C>T r.(?) p.(=)
-?/. - c.-1481T>C r.(?) p.(=)
-?/. - c.-1430G>A r.(?) p.(=)
+?/. - c.-1423T>C r.(?) p.(=)
+/. - c.-1422del r.(?) p.(=)
?/. - c.-1418_-1327del r.(?) p.(=)
+/. - c.-1417G>A r.(?) p.(=)
+/. - c.-1414dup r.(?) p.(=)
+/. - c.-1413T>G r.(?) p.(=)
?/. - c.-1406C>T r.(?) p.(=)
+?/. - c.-1404G>A r.(?) p.(=)
+/. - c.-1402A>T r.(?) p.(=)
+/. - c.-1401T>C r.(?) p.(=)
+/. - c.-1401T>G r.(?) p.(=)
+/. - c.-1401T>G r.(?) p.(=)
+/. - c.-1401T>G r.(?) p.(=)
+/. - c.-1401T>G r.(?) p.(=)
+/. - c.-1400G>T r.(?) p.(=)
?/. - c.-1397C>T r.(?) p.(=)
?/. - c.-1394C>T r.(?) p.(=)
+/. - c.-1379T>A r.(?) p.(=)
+/. - c.-1376C>G r.(?) p.(=)
+/. - c.-1376_-1358del r.(?) p.(=)
+/. - c.-1371G>A r.(?) p.(=)
?/. - c.-1365A>T r.(?) p.(=)
?/. - c.-1364C>G r.(?) p.(=)
?/. - c.-1364C>T r.(?) p.(=)
?/. - c.-1356A>G r.(?) p.(=)
-?/. - c.-1356A>G r.(?) p.(=)
+/. - c.-1345C>G r.(?) p.(=)
+/. - c.-1343T>G r.(?) p.(=)
-?/. - c.-409G>A r.(?) p.(=)
-?/. - c.-4G>C r.(?) p.(=)
-?/. - c.20G>A r.(?) p.(Gly7Glu)
?/. - c.37_54del r.(?) p.(Gly13_Leu18del)
-/. - c.56G>A r.(?) p.(Arg19His)
-/. - c.56G>A r.(?) p.(Arg19His)
-/. - c.57C>A r.(?) p.(Arg19=)
-/. - c.57C>A r.(?) p.(Arg19=)
-?/. - c.57C>A r.(?) p.(Arg19=)
+?/. - c.220G>T r.(?) p.(Glu74*)
+/. 3 c.220G>T r.(?) p.(Glu74Ter)
-/. - c.288T>C r.(?) p.(Ile96=)
-/. - c.349-17T>C r.(=) p.(=)
-?/. - c.394T>C r.(?) p.(Cys132Arg)
-?/. - c.430A>G r.(?) p.(Thr144Ala)
?/. - c.450C>G r.(?) p.(Ile150Met)
?/. - c.523G>C r.(?) p.(Gly175Arg)
?/. - c.548A>T r.(?) p.(His183Leu)
+?/. - c.548A>T r.(?) p.(His183Leu)
+/. - c.556C>T r.(?) p.(Arg186Trp)
+/. - c.556C>T r.(?) p.(Arg186Trp)
+/. - c.556C>T r.(?) p.(Arg186Trp)
+/. - c.556C>T r.(?) p.(Arg186Trp)
?/. - c.557G>A r.(?) p.(Arg186Gln)
+?/. - c.569G>A r.(?) p.(Arg190His)
+/. - c.574dup r.(?) p.(Ala192GlyfsTer27)
-?/. - c.620C>T r.(?) p.(Ala207Val)
+/. - c.700C>T r.(?) p.(Gln234Ter)
-/. - c.716T>A r.(?) p.(Met239Lys)
-/. - c.716T>A r.(?) p.(Met239Lys)
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