Transcript #00006038 (NM_000497.3, CYP11B1 gene)

Transcript name transcript variant 1
Gene name CYP11B1 (cytochrome P450, family 11, subfamily B, polypeptide 1)
Chromosome 8
Transcript - NCBI ID NM_000497.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_000488.3
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

88 entries on 1 page. Showing entries 1 - 88.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Haplotype     
+/. - c.-7_(1121+1_1122-1){0} r.? p.0? -
+/. - c.-7_(1121+1_1122-1){0} r.? p.0? -
+/. - c.-7_(1121+1_1122-1){0} r.? p.0? -
-?/. - c.50C>T r.(?) p.(Ser17Phe) -
+?/. - c.61del r.(?) p.(Ala21HisfsTer30) -
-?/. - c.77C>T r.(?) p.(Thr26Met) -
?/. - c.138C>T r.(?) p.(=) -
?/. - c.172G>A r.(?) p.(Glu58Lys) -
+?/. - c.217C>T r.(?) p.(Gln73*) -
-/. - c.225A>G r.(?) p.(Leu75=) -
-/. - c.225A>G r.(?) p.(Leu75=) -
+/. - c.239+1G>C r.spl p.? -
-/. - c.243C>T r.(?) p.(Tyr81=) -
-/. - c.246C>T r.(?) p.(Asp82=) -
-/. - c.246C>T r.(?) p.(Asp82=) -
?/. - c.363_365del r.(?) p.(Gln121del) -
+?/. - c.385G>A r.(?) p.(Val129Met) -
+?/. - c.388T>C r.(?) p.(Phe130Leu) -
-?/. - c.395+9C>T r.(=) p.(=) -
-/. - c.396-612A>G r.(=) p.(=) -
+?/. - c.400G>C r.(?) p.(Gly134Arg) -
+/. - c.421C>T r.(?) p.(Arg141*) -
-?/. - c.435T>C r.(?) p.(Asn145=) -
-?/. - c.441A>T r.(?) p.(Glu147Asp) -
+/. - c.449C>T r.(?) p.(Ser150Leu) -
-?/. - c.456C>G r.(?) p.(Asn152Lys) -
-?/. - c.456C>G r.(?) p.(Asn152Lys) -
-?/. - c.459T>C r.(?) p.(Ala153=) -
-?/. - c.555C>T r.(?) p.(=) -
+/. - c.595+1G>A r.spl p.? -
-/. - c.595+12G>A r.(=) p.(=) -
-/. - c.595+12G>A r.(=) p.(=) -
+?/. - c.615del r.(?) p.(Phe205Leufs*17) -
+?/. - c.712dup r.(?) p.(Met238Asnfs*21) -
-?/. - c.743C>T r.(?) p.(Thr248Ile) -
+/. - c.793C>T r.(?) p.(Gln265Ter) -
+/. - c.799G>A r.(?) p.(Gly267Ser) -
+/. - c.799G>A r.(?) p.(Gly267Ser) -
+?/. - c.799+5G>C r.spl? p.? -
+/. - c.799+5G>C r.spl? p.? -
?/. - c.800-3T>G r.spl p.? -
-?/. - c.825T>C r.(?) p.(Tyr275=) -
+?/. - c.858C>A r.(?) p.(Tyr286Ter) -
+/. - c.896T>C r.(?) p.(Leu299Pro) -
+?/. - c.907del r.(?) p.(Ala303ProfsTer22) -
+?/. - c.916G>A r.(?) p.(Ala306Thr) -
-?/. - c.930A>G r.(?) p.(=) -
+/. - c.940G>C r.(?) p.(Gly314Arg) -
+?/. - c.945C>A r.(?) p.(Ser315Arg) -
?/. - c.945C>G r.(?) p.(Ser315Arg) -
+/. - c.953C>T r.(?) p.(Thr318Met) -
+/. - c.954G>C r.spl p.(?,Thr318=) -
?/. - c.954+148C>G r.(=) p.(=) -
+/. - c.995G>A r.(?) p.(Arg332Gln) -
-?/. - c.1003A>G r.(?) p.(Asn335Asp) -
-?/. - c.1014G>A r.(?) p.(Gln338=) -
-?/. - c.1014G>A r.(?) p.(Gln338=) -
+?/. 6 c.1027G>A r.(?) p.(Glu343Lys) -
-?/. - c.1064C>T r.(?) p.(Pro355Leu) -
+/. - c.1066C>T r.(?) p.(Gln356*) -
+/. - c.1066C>T r.(?) p.(Gln356*) -
+/. - c.1066C>T r.(?) p.(Gln356*) -
+/. - c.1066C>T r.(?) p.(Gln356*) -
-/. - c.1086G>C r.(?) p.(Leu362=) -
-/. - c.1120C>A r.(?) p.(Arg374=) -
-/. - c.1120C>A r.(?) p.(Arg374=) -
-/. - c.1122-80T>G r.(=) p.(=) -
-?/. - c.1125C>G r.(?) p.(Leu375=) -
+?/. - c.1150_1153del r.(?) p.(Arg384Trpfs*45) -
+/. - c.1150_1153del r.(?) p.(Arg384TrpfsTer45) -
+/. - c.1151G>A r.(?) p.(Arg384Gln) -
-/. - c.1157C>T r.(?) p.(Ala386Val) -
+?/. - c.1219del r.(?) p.(Leu407SerfsTer23) -
-?/. - c.1266C>G r.(?) p.(Arg422=) -
-?/. - c.1272C>T r.(?) p.(Asn424=) -
+?/. - c.1325C>T r.(?) p.(Pro442Leu) -
+?/. - c.1342C>T r.(?) p.(Arg448Cys) -
-/. - c.1353T>C r.(?) p.(Leu451=) -
-?/. - c.1353T>C r.(?) p.(Leu451=) -
+/. - c.1359dup r.(?) p.(Arg454AlafsTer84) -
+?/. - c.1360C>T r.(?) p.(Arg454Cys) -
+/. - c.1360C>T r.(?) p.(Arg454Cys) -
+?/. - c.1388_1393dup r.(?) p.(Leu463_Leu464dup) -
+?/. - c.1391_1393del r.(?) p.(Leu464del) -
+?/. - c.1398+5G>C r.spl? p.? -
?/. - c.1398+5G>C r.spl? p.? -
-/. - c.1399-14G>C r.(=) p.(=) -
-?/. - c.1451T>A r.(?) p.(Val484Asp) -
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