Transcript #00020254 (NM_006946.2, SPTBN2 gene)

Transcript name spectrin, beta, non-erythrocytic 2
Gene name SPTBN2 (spectrin, beta, non-erythrocytic 2)
Chromosome 11
Transcript - NCBI ID NM_006946.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_008877.1
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

248 entries on 3 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.-119C>T r.(?) p.(=)
?/. - c.-22-10C>A r.(=) p.(=)
?/. - c.2T>C r.(?) p.?
?/. - c.92C>T r.(?) p.(Ser31Leu)
-?/. - c.92C>T r.(?) p.(Ser31Leu)
?/. - c.122G>A r.(?) p.(Arg41His)
-?/. - c.157+5G>A r.spl? p.?
-?/. - c.157+5G>A r.spl? p.?
-?/. - c.157+16G>A r.(=) p.(=)
?/. - c.185C>T r.(?) p.(Thr62Ile)
+?/. - c.185C>T r.(?) p.(Thr62Ile)
+?/. - c.193A>C r.(?) p.(Lys65Gln)
?/. - c.224C>T r.(?) p.(Thr75Met)
?/. - c.229C>T r.(?) p.(Arg77Trp)
?/. - c.229C>T r.(?) p.(Arg77Trp)
?/. - c.229C>T r.(?) p.(Arg77Trp)
?/. - c.233T>C r.(?) p.(Val78Ala)
?/. - c.266G>T r.(?) p.(Arg89Leu)
-/. - c.285C>T r.(?) p.(Leu95=)
-?/. - c.363G>A r.(?) p.(Lys121=)
?/. - c.403A>C r.(?) p.(Asn135His)
?/. - c.406A>G r.(?) p.(Met136Val)
?/. - c.406A>G r.(?) p.(Met136Val)
?/. - c.406A>G r.(?) p.(Met136Val)
?/. - c.406A>G r.(?) p.(Met136Val)
+?/. - c.448C>A r.(?) p.(Leu150Ile)
+?/. - c.479T>G r.(?) p.(Phe160Cys)
?/. - c.486C>G r.(?) p.(Ile162Met)
?/. - c.488A>C r.(?) p.(Gln163Pro)
?/. - c.584A>G r.(?) p.(Asn195Ser)
?/. - c.584A>G r.(?) p.(Asn195Ser)
-/. - c.585C>T r.(?) p.(Asn195=)
?/. - c.590A>G r.(?) p.(Asn197Ser)
-?/. - c.611G>C r.(?) p.(Ser204Thr)
?/. - c.656G>A r.(?) p.(Arg219Gln)
-?/. - c.657-3C>T r.spl? p.?
+/. - c.812C>A r.(?) p.(Thr271Asn)
+?/. - c.814T>C r.(?) p.(Tyr272His)
?/. - c.868G>A r.(?) p.(Gly290Ser)
-/. - c.885+5T>C r.spl? p.?
?/. - c.976G>A r.(?) p.(Val326Met)
-?/. - c.1002C>G r.(?) p.(Ala334=)
?/. - c.1073+5G>A r.spl? p.?
?/. - c.1130G>T r.(?) p.(Arg377Leu)
-?/. - c.1153A>G r.(?) p.(Thr385Ala)
-?/. - c.1161C>T r.(?) p.(Arg387=)
?/. - c.1187A>C r.(?) p.(Asn396Thr)
?/. - c.1201C>T r.(?) p.(Arg401Trp)
-?/. - c.1221C>T r.(?) p.(His407=)
-/. - c.1221C>T r.(?) p.(His407=)
?/. - c.1246G>A r.(?) p.(Glu416Lys)
?/. - c.1246G>A r.(?) p.(Glu416Lys)
?/. - c.1246G>A r.(?) p.(Glu416Lys)
?/. - c.1246G>A r.(?) p.(Glu416Lys)
?/. - c.1255C>T r.(?) p.(Arg419Cys)
+?/. - c.1261_1263del r.(?) p.(Glu421del)
?/. - c.1286G>A r.(?) p.(Arg429His)
?/. - c.1294C>T r.(?) p.(Arg432Cys)
+?/. - c.1309C>G r.(?) p.(Arg437Gly)
+?/. - c.1309C>T r.(?) p.(Arg437Trp)
+/. - c.1309C>T r.(?) p.(Arg437Trp)
+/. - c.1309C>T r.(?) p.(Arg437Trp)
+/. - c.1310G>A r.(?) p.(Arg437Gln)
+?/. - c.1310G>A r.(?) p.(Arg437Gln)
-?/. - c.1323C>T r.(?) p.(Leu441=)
-?/. - c.1323C>T r.(?) p.(Leu441=)
-?/. - c.1350+17C>T r.(=) p.(=)
-?/. - c.1351-7G>A r.(=) p.(=)
-?/. - c.1351-7G>A r.(=) p.(=)
-/. - c.1351-7G>T r.(=) p.(=)
-/. - c.1416G>A r.(?) p.(Thr472=)
+/. 12 c.1438C>T r.(?) p.(Arg480Trp)
+/. - c.1438C>T r.(?) p.(Arg480Trp)
+?/. - c.1438C>T r.(?) p.(Arg480Trp)
?/. - c.1438C>T r.(?) p.(Arg480Trp)
+/. 12 c.1438C>T r.(?) p.(Arg480Trp)
+?/. - c.1438C>T r.(?) p.(Arg480Trp)
?/. - c.1456G>A r.(?) p.(Ala486Thr)
-?/. - c.1456G>A r.(?) p.(Ala486Thr)
-?/. - c.1491C>T r.(?) p.(His497=)
?/. - c.1501C>T r.(?) p.(Arg501Cys)
-?/. - c.1504A>G r.(?) p.(Ile502Val)
-?/. - c.1504A>G r.(?) p.(Ile502Val)
?/. - c.1532G>A r.(?) p.(Arg511Gln)
?/. - c.1549C>T r.(?) p.(Arg517Trp)
?/. - c.1550G>A r.(?) p.(Arg517Gln)
-?/. - c.1569G>A r.(?) p.(Arg523=)
-?/. - c.1654-13G>A r.(=) p.(=)
-?/. - c.1654-13G>A r.(=) p.(=)
?/. - c.1676T>C r.(?) p.(Leu559Pro)
-?/. - c.1719C>T r.(?) p.(His573=)
-?/. - c.1722G>A r.(?) p.(Glu574=)
-?/. - c.1722G>A r.(?) p.(Glu574=)
-?/. - c.1807+13C>T r.(=) p.(=)
-?/. - c.1827G>T r.(?) p.(Pro609=)
?/. - c.1877T>C r.(?) p.(Leu626Pro)
?/. - c.1882G>A r.(?) p.(Glu628Lys)
?/. - c.1972C>T r.(?) p.(Arg658Trp)
-?/. - c.1972C>T r.(?) p.(Arg658Trp)
?/. - c.2002G>A r.(?) p.(Asp668Asn)
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