Transcript #00009459 (NM_000190.3, HMBS gene)

Transcript name transcript variant 1
Gene name HMBS (hydroxymethylbilane synthase)
Chromosome 11
Transcript - NCBI ID NM_000190.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_000181.2
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

72 entries on 1 page. Showing entries 1 - 72.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+/. - c.33+1G>A r.spl? p.?
+/. - c.87+5G>A r.spl? p.?
-/. - c.88-14G>A r.(=) p.(=)
-/. - c.88-14G>A r.(=) p.(=)
-/. - c.88-14G>A r.(=) p.(=)
+/. - c.91G>A r.(?) p.(Ala31Thr)
?/. - c.95G>A r.(?) p.(Arg32His)
+/. - c.181dup r.(?) p.(Asp61GlyfsTer5)
+?/. - c.210+2T>A r.(?) p.(?)
+/. - c.219_220del r.(?) p.(Ser75ProfsTer7)
-?/. - c.257A>T r.(?) p.(Glu86Val)
-/. - c.267-56_267-49del r.(=) p.(=)
?/. - c.271G>A r.(?) p.(Asp91Asn)
+/. - c.287C>T r.(?) p.(Ser96Phe)
+/. 7 c.294G>T r.(?) p.(Lys98Asn)
-?/. - c.303C>T r.(?) p.(=)
-?/. - c.345-10C>T r.(=) p.(=)
+/. - c.346C>T r.(?) p.(Arg116Trp)
+?/. - c.427G>A r.(?) p.(Val143Met)
+/. - c.500G>A r.(?) p.(Arg167Gln)
?/. - c.500G>A r.(?) p.(Arg167Gln)
+/. - c.517C>T r.(?) p.(Arg173Trp)
+/. - c.518G>A r.(?) p.(Arg173Gln)
?/. - c.569C>T r.(?) p.(Thr190Ile)
-/. - c.606G>T r.(?) p.(Val202=)
-/. - c.606G>T r.(?) p.(Val202=)
-/. - c.606G>T r.(?) p.(Val202=)
-/. - c.613-19C>A r.(=) p.(=)
-/. - c.613-19C>A r.(=) p.(=)
-/. - c.613-19C>A r.(=) p.(=)
-/. - c.613-19C>A r.(=) p.(=)
+/. - c.635T>G r.(?) p.(Met212Arg)
+/. - c.647G>A r.(?) p.(Gly216Asp)
+/. - c.651+3A>T r.spl? p.?
+/. - c.652-1G>C r.spl? p.?
+/. - c.667G>A r.(?) p.(Glu223Lys)
+/. - c.674G>A r.(?) p.(Arg225Gln)
+?/. - c.674G>A r.(?) p.(Arg225Gln)
?/. - c.674G>A r.(?) p.(Arg225Gln)
+/. - c.701T>C r.(?) p.(Leu234Pro)
+/. - c.716A>G r.(?) p.(His239Arg)
+/. - c.724_743dup r.(?) p.(Ile248MetfsTer14)
+/. - c.730_731del r.(?) p.(Leu244AlafsTer6)
+/. - c.730_731del r.(?) p.(Leu244Alafs*6)
?/. - c.737G>A r.(?) p.(Arg246His)
+/. - c.739T>C r.(?) p.(Cys247Arg)
-?/. - c.765G>C r.(?) p.(Arg255Ser)
+/. - c.791del r.(?) p.(Pro264GlnfsTer2)
+/. - c.825+1G>A r.spl? p.?
?/. - c.858C>A r.(?) p.(Asp286Glu)
-?/. - c.858C>T r.(?) p.(Asp286=)
-?/. - c.912+5C>T r.spl? p.?
-?/. - c.912+19G>A r.(=) p.(=)
-?/. - c.912+19G>A r.(=) p.(=)
-/. - c.913-27C>G r.(=) p.(=)
-?/. - c.962G>A r.(?) p.(Arg321His)
-?/. - c.962G>A r.(?) p.(Arg321His)
+/. - c.991G>A r.(?) p.(Ala331Thr)
-?/. - c.1020C>T r.(?) p.(=)
?/. - c.1064G>A r.(?) p.(Arg355Gln)
-?/. - c.1075G>A r.(?) p.(Asp359Asn)
+?/. 14 c.1084del r.(?) p.(*362Asnext*?)
-/. - c.*3765T>C r.(=) p.(=)
-/. - c.*3765T>C r.(=) p.(=)
?/. - c.*3895A>C r.(=) p.(=)
?/. - c.*3943_*3945del r.(=) p.(=)
+?/. - c.*4197C>T r.(=) p.(=)
?/. - c.*4273G>T r.(=) p.(=)
-?/. - c.*4565C>T r.(=) p.(=)
?/. - c.*4669T>A r.(=) p.(=)
+/. - c.*4756_*4757del r.(=) p.(=)
?/. - c.*5181A>C r.(=) p.(=)
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