Transcript #00011720 (NM_000528.3, MAN2B1 gene)

Transcript name transcript variant 1
Gene name MAN2B1 (mannosidase, alpha, class 2B, member 1)
Chromosome 19
Transcript - NCBI ID NM_000528.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_000519.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

195 entries on 2 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.-2689A>G r.(?) p.(=)
-?/. - c.19G>C r.(?) p.(Ala7Pro)
-?/. - c.48G>A r.(?) p.(Leu16=)
-?/. - c.48G>A r.(?) p.(Leu16=)
+/. - c.65G>A r.(?) p.(Trp22*)
-?/. - c.160-7T>C r.(=) p.(=)
+/? ? c.164G>T r.(?) p.(Cys55Phe)
?/. - c.179C>T r.(?) p.(Pro60Leu)
+/? 2 c.215A>T r.215a>u p.His72Leu
+/? 2 c.215A>T r.215a>u p.His72Leu
+/? 2 c.215A>T r.215a>u p.His72Leu
+/? 2 c.215A>T r.215a>u p.His72Leu
+/? 2 c.215A>T r.215a>u p.His72Leu
+/? ? c.215A>T r.(?) p.(His72Leu)
+/? ? c.222C>A r.(?) p.(Asp74Glu)
+/. - c.231G>A r.(?) p.(Trp77Ter)
+?/. - c.262+2T>G r.spl? p.?
+?/. - c.262+3G>C r.spl? p.?
+/? ? c.283G>C r.(?) p.(Ala95Pro)
+/? ? c.295T>C r.(?) p.(Tyr99His)
+?/. - c.308C>T r.(?) p.(Ser103Leu)
?/. - c.376C>T r.(?) p.(Arg126Cys)
+/. 3 c.418C>T r.(?) p.(Arg140Ter)
?/. - c.455A>G r.(?) p.(Asn152Ser)
+/? ? c.475G>A r.(?) p.(Asp159Asn)
-?/. - c.552C>A r.(?) p.(Gly184=)
+/? ? c.590C>G r.(?) p.(Pro197Arg)
+?/. - c.595G>T r.(?) p.(Gly199Cys)
+/? ? c.598C>A r.(?) p.(His200Asn)
+/? ? c.599A>T r.(?) p.(His200Leu)
+/? ? c.599A>T r.(?) p.(His200Leu)
+/? ? c.605G>C r.(?) p.(Arg202Pro)
-/. - c.619C>T r.(?) p.(Leu207=)
+/? ? c.685C>T r.(?) p.(Arg229Trp)
-/. - c.719G>A r.(?) p.(Arg240Gln)
-?/. - c.743C>T r.(?) p.(Pro248Leu)
-?/. - c.743C>T r.(?) p.(Pro248Leu)
-?/. - c.743C>T r.(?) p.(Pro248Leu)
?/. - c.743C>T r.(?) p.(Pro248Leu)
-?/. - c.744G>A r.(?) p.(Pro248=)
-/. - c.747C>T r.(?) p.(Thr249=)
-/. - c.748G>T r.(?) p.(Ala250Ser)
?/. - c.749C>T r.(?) p.(Ala250Val)
+/. - c.763+2_763+8del r.spl p.?
-?/. - c.779G>T r.(?) p.(Gly260Val)
+/? ? c.788C>T r.(?) p.(Pro263Leu)
-?/. - c.789G>A r.(?) p.(Pro263=)
?/. - c.823G>A r.(?) p.(Asp275Asn)
-/. - c.832C>G r.(?) p.(Leu278Val)
-/. - c.832C>G r.(?) p.(Leu278Val)
-?/. - c.844C>T r.(?) p.(Pro282Ser)
-?/. - c.844C>T r.(?) p.(Pro282Ser)
-?/. - c.844C>T r.(?) p.(Pro282Ser)
-?/. - c.844C>T r.(?) p.(Pro282Ser)
-/. - c.935C>A r.(?) p.(Thr312Asn)
-?/. - c.935C>A r.(?) p.(Thr312Asn)
-/. - c.935C>T r.(?) p.(Thr312Ile)
-/? 7 c.935C>T r.935c>u p.Thr312Ile
-/? 7 c.935C>T r.935c>u p.Thr312Ile
-/? 7 c.935C>T r.935c>u p.Thr312Ile
-/? 7 c.935C>T r.935c>u p.Thr312Ile
+/? 7 c.935C>T r.935c>u p.Thr312Ile
-/? 7 c.935C>T r.935c>u p.Thr312Ile
-/? 7 c.935C>T r.(=) p.(Thr312Ile)
-/. - c.935C>T r.(?) p.(Thr312Ile)
+/? ? c.953C>T r.(?) p.(Ser318Leu)
-/. - c.1010G>A r.(?) p.(Arg337Gln)
-/. - c.1010G>A r.(?) p.(Arg337Gln)
+?/. - c.1026+2T>G r.spl? p.?
+/. - c.1026+2T>G r.spl? p.?
?/. - c.1026+2T>G r.spl? p.?
-?/. - c.1026+8C>T r.(=) p.(=)
+/? ? c.1055T>C r.(?) p.(Leu352Pro)
-?/. - c.1059C>T r.(?) p.(Tyr353=)
+/? ? c.1063A>C r.(?) p.(Thr355Pro)
+/? ? c.1067C>G r.(?) p.(Pro356Arg)
-/. - c.1068C>G r.(?) p.(Pro356=)
-?/. - c.1068C>G r.(?) p.(Pro356=)
-?/. - c.1110-8C>T r.(=) p.(=)
-?/. - c.1110-4G>A r.spl? p.?
+/? ? c.1136C>T r.(?) p.(Pro379Leu)
?/. - c.1154A>G r.(?) p.(His385Arg)
-/. - c.1158G>A r.(?) p.(Gln386=)
-?/. - c.1158G>A r.(?) p.(Gln386=)
+/? ? c.1168G>T r.(?) p.(Gly390Cys)
?/. - c.1183C>T r.(?) p.(Arg395Trp)
?/. - c.1204G>A r.(?) p.(Glu402Lys)
?/. - c.1204G>A r.(?) p.(Glu402Lys)
?/. - c.1204G>A r.(?) p.(Glu402Lys)
+/? ? c.1204G>A r.(?) p.(Glu402Lys)
-?/. - c.1209C>A r.(?) p.(Arg403=)
?/. - c.1213A>G r.(?) p.(Ser405Gly)
-?/. - c.1231-13C>T r.(=) p.(=)
-/. - c.1238A>G r.(?) p.(Asn413Ser)
-?/. - c.1250C>G r.(?) p.(Ala417Gly)
+/? ? c.1259G>T r.(?) p.(Gly420Val)
-?/. - c.1309+10G>A r.(=) p.(=)
+/? ? c.1333C>T r.(?) p.(His445Tyr)
+/? ? c.1351G>T r.(?) p.(Gly451Cys)
+/? ? c.1358C>A r.(?) p.(Ser453Tyr)
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