Transcript #00025682 (NM_006715.3, MAN2C1 gene)

Transcript name transcript variant 1
Gene name MAN2C1 (mannosidase, alpha, class 2C, member 1)
Chromosome 15
Transcript - NCBI ID NM_006715.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_006706.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2022-01-21 14:49:04 +01:00 (CET)
Date last edited N/A


Variants

60 entries on 1 page. Showing entries 1 - 60.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.-3598A>G r.(?) p.(=)
-?/. - c.-3547G>A r.(?) p.(=)
-?/. - c.-3538C>T r.(?) p.(=)
?/. - c.-3514T>G r.(?) p.(=)
-?/. - c.101+6G>A r.(=) p.(=)
?/. - c.183G>C r.(?) p.(Gln61His)
-?/. - c.227+7A>T r.(=) p.(=)
?/. - c.280G>A r.(?) p.(Gly94Ser)
-?/. - c.332G>A r.(?) p.(Arg111His)
+?/. - c.422+1G>A r.spl? p.?
+?/. - c.422+1G>A r.spl? p.?
?/. - c.475G>A r.(?) p.(Gly159Arg)
?/. - c.490G>A r.(?) p.(Ala164Thr)
?/. - c.506_508del r.(?) p.(Lys169del)
?/. - c.547C>A r.(?) p.(=)
+?/. - c.601-2A>G r.spl? p.?
+/. 6i c.601-2A>G r.601_709del p.Gly201AlafsTer11
+/. 6i c.601-2A>G r.601_709del p.Gly201AlafsTer11
+/. 6i c.601-2A>G r.601_709del p.Gly201AlafsTer11
+?/. - c.607G>A r.(?) p.(Gly203Arg)
+/. - c.607G>A r.(?) p.(Gly203Arg)
?/. - c.810A>G r.(?) p.(=)
?/. - c.811G>A r.(?) p.(Glu271Lys)
?/. - c.1008+6T>G r.(=) p.(=)
?/. - c.1165A>T r.(?) p.(Ile389Phe)
?/. - c.1167C>G r.(?) p.(Ile389Met)
?/. - c.1273C>G r.(?) p.(Pro425Ala)
-?/. - c.1327G>A r.(?) p.(Val443Met)
?/. - c.1402C>T r.(?) p.(Pro468Ser)
+/. - c.1461-2A>G r.spl? p.?
?/. - c.1583A>T r.(?) p.(Gln528Leu)
-?/. - c.1584+4_1584+5del r.spl? p.?
?/. - c.1739T>C r.(?) p.(Val580Ala)
?/. - c.1792+4A>G r.spl? p.?
?/. - c.1792+4A>G r.spl? p.?
?/. - c.2047-18A>G r.(=) p.(=)
?/. - c.2197C>T r.(?) p.(Pro733Ser)
?/. - c.2197C>T r.(?) p.(Pro733Ser)
+/. - c.2303G>A r.(?) p.(Arg768Gln)
+/. - c.2303G>A r.(?) p.(Arg768Gln)
-?/. - c.2403+9G>C r.(=) p.(=)
?/. - c.2576C>T r.(?) p.(Ser859Leu)
?/. - c.2584G>A r.(?) p.(Gly862Ser)
?/. - c.2602C>T r.(?) p.(Leu868Phe)
+/. - c.2612G>C r.(?) p.(Cys871Ser)
+/. - c.2612G>C r.(?) p.(Cys871Ser)
+/. - c.2612G>C r.(?) p.(Cys871Ser)
?/. - c.2618A>G r.(?) p.(Tyr873Cys)
?/. - c.2663G>A r.(?) p.(Arg888Gln)
+/. - c.2733_2734del r.(?) p.(His911GlnfsTer67)
+/. - c.2733_2734del r.(?) p.(His911GlnfsTer67)
?/. - c.2774A>G r.(?) p.(Tyr925Cys)
-?/. - c.2878G>A r.(?) p.(Val960Ile)
?/. - c.2888C>T r.(?) p.(Ala963Val)
?/. - c.2890_2900dup r.(?) p.(Gln968Argfs*11)
+?/. - c.2912C>T r.(?) p.(Ser971Leu)
-?/. - c.2996+10G>A r.(=) p.(=)
-?/. - c.2997-8T>C r.(=) p.(=)
-?/. - c.3017C>G r.(?) p.(Pro1006Arg)
?/. - c.*3700T>A r.(=) p.(=)
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