Transcript #00000646 (NM_015073.1, SIPA1L3 gene)

Transcript name signal-induced proliferation-associated 1 like 3
Gene name SIPA1L3 (signal-induced proliferation-associated 1 like 3)
Chromosome 19
Transcript - NCBI ID NM_015073.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_055888.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2012-09-13 12:43:31 +02:00 (CEST)
Date last edited N/A


Variants

59 entries on 1 page. Showing entries 1 - 59.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. 1i c.-378-48313A>G r.(=) p.(=)
-?/. 1i c.-378-46804G>A r.(=) p.(=)
?/. - c.181_192del r.(?) p.(Ala61_Thr64del)
?/. - c.187_192del r.(?) p.(Ala63_Thr64del)
-/. - c.187_192dup r.(?) p.(Ala63_Thr64dup)
-?/. - c.339G>A r.(?) p.(Met113Ile)
-?/. - c.341C>A r.(?) p.(Ala114Asp)
?/. - c.473C>G r.(?) p.(Ser158Cys)
?/. - c.548_567dup r.(?) p.(Ala190ThrfsTer40)
-/. - c.572G>A r.(?) p.(Arg191Gln)
+?/. - c.611dup r.(?) p.(Ser204ArgfsTer215)
?/. - c.765_767dup r.(?) p.(Gly256dup)
-?/. - c.788A>G r.(?) p.(Asn263Ser)
-?/. - c.820C>G r.(?) p.(Leu274Val)
-?/. - c.953C>T r.(?) p.(Pro318Leu)
-?/. - c.978C>G r.(?) p.(Ser326Arg)
-?/. - c.1017C>T r.(?) p.(Ser339=)
-?/. - c.1128C>T r.(?) p.(Ser376=)
?/. - c.1149_1160dup r.(?) p.(Leu384_Ser387dup)
-/. - c.1245C>T r.(?) p.(Leu415=)
-?/. - c.1389C>G r.(?) p.(Ala463=)
-?/. - c.1422G>C r.(?) p.(Ser474=)
-?/. - c.1464G>T r.(?) p.(Arg488=)
?/. - c.1510T>C r.(?) p.(Tyr504His)
?/. - c.1679G>A r.(?) p.(Arg560Gln)
-?/. - c.2115C>T r.(?) p.(Thr705=)
-?/. - c.2172G>T r.(?) p.(Thr724=)
-?/. - c.2292-6C>T r.(=) p.(=)
-?/. - c.2328C>T r.(?) p.(Phe776=)
?/. - c.2332C>A r.(?) p.(Pro778Thr)
?/. - c.2386T>A r.(?) p.(Leu796Met)
?/. - c.2446A>G r.(?) p.(Met816Val)
?/. - c.2658C>G r.(?) p.(Ile886Met)
-?/. - c.2790T>C r.(?) p.(Tyr930=)
-?/. - c.3061G>A r.(?) p.(Asp1021Asn)
-?/. - c.3144-6C>A r.(=) p.(=)
-?/. - c.3176C>T r.(?) p.(Ser1059Leu)
?/. - c.3368G>A r.(?) p.(Arg1123Gln)
-?/. - c.3492C>G r.(?) p.(Pro1164=)
?/. - c.3643A>G r.(?) p.(Met1215Val)
?/. - c.3869C>T r.(?) p.(Pro1290Leu)
-?/. - c.3942C>G r.(?) p.(Thr1314=)
-?/. - c.3994G>A r.(?) p.(Ala1332Thr)
?/. - c.4009C>G r.(?) p.(Pro1337Ala)
-?/. - c.4051G>T r.(?) p.(Ala1351Ser)
-?/. - c.4111G>A r.(?) p.(Gly1371Ser)
-?/. - c.4212C>T r.(?) p.(Asp1404=)
+/. 17 c.4489C>T r.(?) p.(Arg1497*)
+/. 17 c.4489C>T r.(?) p.(Arg1497*)
+/. 17 c.4489C>T r.(?) p.(Arg1497*)
+/. 17 c.4489C>T r.(?) p.(Arg1497*)
?/. - c.4507C>T r.(?) p.(Arg1503Trp)
-?/. - c.4710C>T r.(?) p.(Asp1570=)
?/. - c.4760G>A r.(?) p.(Arg1587His)
?/. - c.4808C>G r.(?) p.(Pro1603Arg)
-?/. - c.4812C>T r.(?) p.(Ala1604=)
?/. - c.4865C>T r.(?) p.(Ser1622Leu)
?/. - c.5030G>A r.(?) p.(Ser1677Asn)
-?/. - c.5052C>T r.(?) p.(His1684=)
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