Transcript #00020253 (NM_003128.2, SPTBN1 gene)

Transcript name transcript variant 1
Gene name SPTBN1 (spectrin, beta, non-erythrocytic 1)
Chromosome 2
Transcript - NCBI ID NM_003128.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_003119.2
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

68 entries on 1 page. Showing entries 1 - 68.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/. - c.-27083295_*7185475dup r.0? p.0?
?/. - c.-48+28507C>A r.(=) p.(=)
-?/. - c.148+32330C>A r.(=) p.(=)
-?/. - c.148+32331C>A r.(=) p.(=)
?/. - c.221G>A r.(?) p.(Arg74Gln)
-?/. - c.474+3A>G r.spl? p.?
?/. - c.475-1G>A r.spl? p.?
?/. - c.533C>G r.(?) p.(Ala178Gly)
+?/. - c.546_548del r.(?) p.(Trp182del)
?/. - c.647G>A r.(?) p.(Arg216Gln)
?/. - c.658A>G r.(?) p.(Ile220Val)
+?/. - c.748C>G r.(?) p.(Leu250Val)
-?/. - c.877-4C>G r.spl? p.?
-?/. - c.954T>A r.(?) p.(=)
-?/. - c.995A>G r.(?) p.(Asn332Ser)
?/. - c.1231C>T r.(?) p.(Arg411Trp)
?/. - c.1246A>G r.(?) p.(Arg416Gly)
+?/. 11 c.1261_1291delinsC r.(?) p.(Glu421_Ala431delinsPro)
+?/. - c.1318G>T r.(?) p.(Glu440*)
-?/. - c.1502C>T r.(?) p.(Ala501Val)
-?/. - c.1502C>T r.(?) p.(Ala501Val)
?/. - c.1502C>T r.(?) p.(Ala501Val)
?/. - c.1670G>A r.(?) p.(Gly557Asp)
?/. - c.1804A>C r.(?) p.(Lys602Gln)
-?/. - c.1898G>A r.(?) p.(Arg633His)
?/. - c.1964G>T r.(?) p.(Arg655Leu)
-?/. - c.2808-9C>T r.(=) p.(=)
-?/. - c.2808G>A r.(?) p.(Arg936=)
+?/. - c.3007C>T r.(?) p.(Arg1003Trp)
-?/. - c.3030A>G r.(?) p.(=)
+?/. 16 c.3160C>T r.(?) p.(Arg1054Ter)
?/. - c.3227C>T r.(?) p.(Ser1076Phe)
?/. - c.3497C>A r.(?) p.(Ser1166Tyr)
+/. 17 c.3593C>T r.(?) p.(Pro1198Leu)
?/. - c.3710G>A r.(?) p.(Ser1237Asn)
-?/. - c.3734G>A r.(?) p.(Arg1245His)
-?/. - c.3765C>G r.(?) p.(Asp1255Glu)
?/. - c.4192G>A r.(?) p.(Gly1398Ser)
?/. - c.4201A>T r.(?) p.(Ser1401Cys)
?/. - c.4318C>G r.(?) p.(Gln1440Glu)
?/. - c.4643G>A r.(?) p.(Ser1548Asn)
?/. - c.5003G>A r.(?) p.(Arg1668His)
?/. - c.5200dup r.(?) p.(Thr1734Asnfs*31)
-?/. - c.5270C>T r.(?) p.(Thr1757Met)
?/. - c.5300A>G r.(?) p.(Asn1767Ser)
?/. - c.5365G>A r.(?) p.(Asp1789Asn)
?/. - c.5453T>C r.(?) p.(Phe1818Ser)
?/. - c.5578-2A>G r.spl? p.?
?/. - c.5711G>A r.(?) p.(Arg1904Lys)
+?/. - c.5730_5731del r.(?) p.(Asp1912Glnfs*35)
+?/. - c.5823-1G>C r.spl? p.?
?/. - c.6001G>A r.(?) p.(Glu2001Lys)
?/. - c.6001G>A r.(?) p.(Glu2001Lys)
-?/. - c.6145G>A r.(?) p.(Val2049Met)
?/. - c.6221_6222del r.(?) p.(Ser2074Cysfs*61)
-?/. - c.6288G>A r.(?) p.(Arg2096=)
?/. - c.6299C>A r.(?) p.(Pro2100Gln)
?/. - c.6299C>A r.(?) p.(Pro2100Gln)
-?/. - c.6309C>T r.(?) p.(=)
-?/. - c.6345C>T r.(?) p.(=)
?/. - c.6380T>C r.(?) p.(Val2127Ala)
?/. - c.6460G>A r.(?) p.(Ala2154Thr)
-?/. - c.6833+10G>A r.(=) p.(=)
-?/. - c.6959C>T r.(?) p.(Thr2320Met)
-?/. - c.6959C>T r.(?) p.(Thr2320Met)
-?/. - c.6974G>A r.(?) p.(Arg2325His)
+?/. - c.7048G>C r.(?) p.(Glu2350Gln)
?/. - c.7053_7064del r.(?) p.(Asp2352_Lys2355del)
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