Transcript #00006039 (NM_000498.3, CYP11B2 gene)

Transcript name cytochrome P450, family 11, subfamily B, polypeptide 2
Gene name CYP11B2 (cytochrome P450, family 11, subfamily B, polypeptide 2)
Chromosome 8
Transcript - NCBI ID NM_000498.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_000489.3
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

56 entries on 1 page. Showing entries 1 - 56.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Haplotype     
+?/. - c.3G>A r.(?) p.0? -
-?/. - c.85G>A r.(?) p.(Ala29Thr) -
-/. - c.89G>A r.(?) p.(Arg30Gln) -
-?/. - c.111G>A r.(?) p.(Pro37=) -
-?/. - c.282G>A r.(?) p.(Pro94=) -
-?/. - c.282G>A r.(?) p.(Pro94=) -
?/. - c.400G>A r.(?) p.(Gly134Arg) -
+?/. - c.422G>A r.(?) p.(Arg141Gln) -
-?/. - c.435C>T r.(?) p.(Asn145=) -
-?/. - c.441T>A r.(?) p.(Asp147Glu) -
-?/. - c.456G>C r.(?) p.(Lys152Asn) -
-?/. - c.459C>T r.(?) p.(Ala153=) -
+?/. - c.493G>A r.(?) p.(Ala165Thr) -
-/. - c.504C>T r.(?) p.(Phe168=) -
-/. - c.504C>T r.(?) p.(Phe168=) -
-/. - c.518A>G r.(?) p.(Lys173Arg) -
-/. - c.518A>G r.(?) p.(Lys173Arg) -
+/. - c.554C>T r.(?) p.(Thr185Ile) -
+/. - c.554C>T r.(?) p.(Thr185Ile) -
-?/. - c.595+11T>C r.(=) p.(=) -
-?/. - c.595+12G>A r.(=) p.(=) -
-?/. - c.595+13C>T r.(=) p.(=) -
-?/. - c.601A>G r.(?) p.(Asn201Asp) -
-/. - c.606A>G r.(?) p.(Leu202=) -
-?/. - c.606A>G r.(?) p.(Leu202=) -
-?/. - c.679C>T r.(?) p.(Leu227=) -
-?/. - c.743T>C r.(?) p.(Ile248Thr) -
-?/. - c.743T>C r.(?) p.(Ile248Thr) -
-?/. - c.743T>C r.(?) p.(Ile248Thr) -
+/. - c.760A>T r.(?) p.(Lys254Ter) -
+/. - c.763G>T r.(?) p.(Glu255Ter) -
-?/. - c.798C>T r.(?) p.(Tyr266=) -
-?/. - c.842A>G r.(?) p.(Asn281Ser) -
-/. - c.873G>A r.(?) p.(Ala291=) -
-/. - c.873G>A r.(?) p.(Ala291=) -
-/. - c.891G>A r.(?) p.(Ala297=) -
-?/. - c.954+9A>G r.(=) p.(=) -
?/. - c.1006G>A r.(?) p.(Val336Met) -
-/. - c.1015A>G r.(?) p.(Ile339Val) -
-/. - c.1016T>A r.(?) p.(Ile339Asn) -
-/. - c.1016T>C r.(?) p.(Ile339Thr) -
-?/. - c.1098G>T r.(?) p.(Arg366=) -
-/. - c.1120C>A r.(?) p.(Arg374=) -
-/. - c.1120C>A r.(?) p.(Arg374=) -
-/. - c.1120C>A r.(?) p.(Arg374=) -
-/. - c.1122-20A>G r.(=) p.(=) -
-?/. - c.1157T>C r.(?) p.(Val386Ala) -
-/. - c.1157T>C r.(?) p.(Val386Ala) -
-?/. - c.1201-19T>C r.(=) p.(=) -
+?/. - c.1342C>T r.(?) p.(Arg448Cys) -
+/. - c.1350C>A r.(?) p.(Cys450Ter) -
+/. - c.1351C>T r.(?) p.(Leu451Phe) -
-?/. - c.1353C>T r.(?) p.(Leu451=) -
+/. - c.1382T>C r.(?) p.(Leu461Pro) -
+?/. - c.1398+1G>A r.spl p.? -
-?/. - c.*81G>A r.(=) p.(=) -
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