Transcript #00025744 (NM_152618.2, BBS12 gene)

Transcript name transcript variant 2
Gene name BBS12 (Bardet-Biedl syndrome 12)
Chromosome 4
Transcript - NCBI ID NM_152618.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_689831.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2022-10-04 12:37:01 +02:00 (CEST)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-/. - c.-124G>A r.(?) p.(=)
-/. - c.51A>G r.(?) p.(Gln17=)
+?/. - c.56T>G r.(?) p.(Leu19Arg)
-?/. - c.58T>C r.(?) p.(Ser20Pro)
?/. - c.67G>A r.(?) p.(Ala23Thr)
?/. - c.67G>A r.(?) p.(Ala23Thr)
?/. - c.68C>T r.(?) p.(Ala23Val)
-?/. - c.75A>G r.(?) p.(Thr25=)
-?/. - c.105A>T r.(?) p.(Ser35=)
-/. - c.116T>C r.(?) p.(Ile39Thr)
-/. - c.116T>C r.(?) p.(Ile39Thr)
?/. - c.116T>C r.(?) p.(Ile39Thr)
?/. - c.116T>C r.(?) p.(Ile39Thr)
?/. - c.116T>C r.(?) p.(Ile39Thr)
-?/. - c.212A>G r.(?) p.(Asn71Ser)
-?/. - c.212A>G r.(?) p.(Asn71Ser)
-?/. - c.212A>G r.(?) p.(Asn71Ser)
?/. - c.274G>A r.(?) p.(Val92Ile)
-?/. - c.355G>A r.(?) p.(Gly119Ser)
-/. - c.355G>A r.(?) p.(Gly119Ser)
-/. - c.378G>T r.(?) p.(Glu126Asp)
?/. - c.577C>T r.(?) p.(Pro193Ser)
+/. - c.670dup r.(?) p.(Thr224AsnfsTer12)
-?/. - c.714T>G r.(?) p.(Asn238Lys)
-/. - c.714T>G r.(?) p.(Asn238Lys)
-?/. - c.714T>G r.(?) p.(Asn238Lys)
+?/. - c.787dup r.(?) p.(Tyr263Leufs*4)
+?/. - c.787dup r.(?) p.(Tyr263Leufs*4)
+?/. - c.787dup r.(?) p.(Tyr263Leufs*4)
+?/. - c.787dup r.(?) p.(Tyr263Leufs*4)
+/. - c.789C>A r.(?) p.(Tyr263Ter)
+?/. - c.807dup r.(?) p.(Glu270Argfs*42)
+?/. - c.898C>T r.(?) p.(Gln300*)
+/. - c.898C>T r.(?) p.(Gln300*)
?/. - c.1003A>G r.(?) p.(Ile335Val)
-?/. - c.1011T>C r.(?) p.(Val337=)
+?/. - c.1055A>C r.(?) p.(Gln352Pro)
+?/. - c.1055A>C r.(?) p.(Gln352Pro)
-/. - c.1062G>C r.(?) p.(Val354=)
-/. - c.1062G>C r.(?) p.(Val354=)
+?/. - c.1063C>T r.(?) p.(Arg355*)
+?/. - c.1063C>T r.(?) p.(Arg355*)
?/. - c.1067T>G r.(?) p.(Ile356Arg)
?/. - c.1092del r.(?) p.(Glu365Argfs*18)
?/. - c.1102C>T r.(?) p.(Arg368Cys)
-/. - c.1103G>A r.(?) p.(Arg368His)
-/. - c.1103G>A r.(?) p.(Arg368His)
+/. - c.1115_1116del r.(?) p.(Phe372Ter)
?/. - c.1115_1116del r.(?) p.(Phe372Ter)
+/. - c.1115_1116del r.(?) p.(Phe372Ter)
+/. - c.1115_1116del r.(?) p.(Phe372Ter)
+?/. - c.1115_1116del r.(?) p.(Phe372*)
+?/. - c.1156C>T r.(?) p.(Arg386Trp)
-/. - c.1157G>A r.(?) p.(Arg386Gln)
-/. - c.1157G>A r.(?) p.(Arg386Gln)
-/. - c.1157G>A r.(?) p.(Arg386Gln)
-/. - c.1200G>A r.(?) p.(Val400=)
-/. - c.1200G>A r.(?) p.(Val400=)
-?/. - c.1207G>A r.(?) p.(Val403Met)
-?/. - c.1207G>A r.(?) p.(Val403Met)
-/. - c.1209G>A r.(?) p.(Val403=)
-?/. - c.1209G>A r.(=) p.(=)
-/. - c.1209G>A r.(?) p.(Val403=)
+?/. - c.1237C>G r.(?) p.(Leu413Val)
+?/. - c.1276T>C r.(?) p.(Cys426Arg)
-/. - c.1286G>C r.(?) p.(Ser429Thr)
-/. - c.1286G>C r.(?) p.(Ser429Thr)
-?/. - c.1287T>C r.(?) p.(Ser429=)
-/. - c.1302C>T r.(?) p.(Ile434=)
-/. - c.1380G>C r.(?) p.(Val460=)
-/. - c.1380G>C r.(?) p.(Val460=)
-/. - c.1380G>C r.(?) p.(Val460=)
-?/. - c.1380G>C r.(=) p.(=)
-/. - c.1381A>C r.(?) p.(Asn461His)
-/. - c.1381A>C r.(?) p.(Asn461His)
-/. - c.1398C>T r.(?) p.(Gly466=)
-/. - c.1398C>T r.(?) p.(Gly466=)
-/. - c.1399G>A r.(?) p.(Asp467Asn)
-/. - c.1399G>A r.(?) p.(Asp467Asn)
-/. - c.1399G>A r.(?) p.(Asp467Asn)
?/. - c.1402G>A r.(?) p.(Gly468Arg)
-/. - c.1410C>T r.(?) p.(Cys470=)
-/. - c.1410C>T r.(?) p.(Cys470=)
-/. - c.1410C>T r.(?) p.(Cys470=)
-/. - c.1451G>A r.(?) p.(Arg484Lys)
-/. - c.1451G>A r.(?) p.(Arg484Lys)
-/. - c.1451G>A r.(?) p.(Arg484Lys)
?/. - c.1499T>C r.(?) p.(Val500Ala)
+/. - c.1502C>T r.(?) p.(Thr501Met)
+?/. - c.1504G>T r.(?) p.(Ala502Ser)
+/. - c.1531C>T r.(?) p.(Gln511Ter)
+?/. - c.1531_1539del r.(?) p.(Gln511_Gln513del)
-?/. - c.1554G>A r.(?) p.(Arg518=)
?/. - c.1571A>G r.(?) p.(Tyr524Cys)
-?/. - c.1611T>C r.(?) p.(Leu537=)
?/. - c.1627G>A r.(?) p.(Glu543Lys)
?/. - c.1681_1683del r.(?) p.(Glu561del)
-?/. - c.1702T>C r.(?) p.(Trp568Arg)
+/. - c.1793A>G r.(?) p.(Tyr598Cys)
-/. - c.1847G>A r.(?) p.(Ser616Asn)
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