Transcript #00024019 (NM_014989.5, RIMS1 gene)

Transcript name transcript variant 1
Gene name RIMS1 (regulating synaptic membrane exocytosis 1)
Chromosome 6
Transcript - NCBI ID NM_014989.5
Transcript - Ensembl ID -
Protein - NCBI ID NP_055804.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2015-02-27 17:44:45 +01:00 (CET)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-/. - c.-20G>C r.(?) p.(=)
?/. - c.? r.(?) p.?
?/. - c.? r.(?) p.?
?/. - c.? r.(?) p.?
?/. - c.? r.(?) p.?
?/. - c.? r.(?) p.?
?/. - c.? r.(?) p.?
?/. - c.2T>C r.(?) p.(Met1?)
?/. - c.28C>T r.(?) p.(Pro10Ser)
-?/. - c.28C>T r.(?) p.(Pro10Ser)
?/. - c.46C>T r.(?) p.(Pro16Ser)
-/. - c.164+16C>T r.(=) p.(=)
-?/. - c.186G>A r.(?) p.(Ala62=)
?/. - c.228G>T r.(?) p.(Gln76His)
-?/. - c.402T>C r.(?) p.(Tyr134=)
-/. - c.438C>T r.(?) p.(Arg146=)
?/. - c.458A>C r.(?) p.(Asn153Thr)
?/. 3 c.458A>C r.(?) p.(Asn153Thr)
-/. - c.648G>A r.(?) p.(Ser216=)
-/. - c.666A>G r.(?) p.(Leu222=)
?/. - c.674C>T r.(?) p.(Ala225Val)
-?/. - c.708C>T r.(?) p.(Ser236=)
-?/. - c.798A>G r.(?) p.(Glu266=)
?/. - c.843T>A r.(?) p.(Asn281Lys)
-/. - c.915C>G r.(?) p.(Val305=)
?/. - c.928C>T r.(?) p.(Arg310Cys)
-/. - c.942G>A r.(?) p.(Arg314=)
?/. - c.976G>A r.(?) p.(Asp326Asn)
?/. - c.1047_1049del r.(?) p.(Glu349del)
-/. - c.1083A>G r.(?) p.(Leu361=)
?/. - c.1094C>T r.(?) p.(Pro365Leu)
-?/. - c.1100A>C r.(?) p.(Lys367Thr)
?/. - c.1106_1107delinsGA r.(?) p.(Pro369Arg)
-?/. - c.1122G>A r.(?) p.(Gln374=)
-/. - c.1182G>C r.(?) p.(Ala394=)
-/. - c.1209G>A r.(?) p.(Ala403=)
-/. - c.1230C>G r.(?) p.(Gly410=)
-?/. - c.1265C>T r.(?) p.(Pro422Leu)
-?/. - c.1305G>C r.(?) p.(Glu435Asp)
?/. - c.1372C>T r.(?) p.(Pro458Ser)
-?/. - c.1459G>A r.(?) p.(Ala487Thr)
-/. - c.1459G>A r.(?) p.(Ala487Thr)
?/. - c.1626G>C r.(?) p.(Glu542Asp)
?/. 6 c.1666G>T r.(?) p.(Val556Phe)
?/. - c.1669A>T r.(?) p.(Ser557Cys)
-?/. - c.1678+7G>C r.(=) p.(=)
-?/. - c.1679-20579A>G r.(=) p.(=)
?/. - c.1679-20577C>G r.(=) p.(=)
-/. - c.1679-16597C>T r.(=) p.(=)
-?/. - c.1776G>A r.(?) p.(Glu592=)
-?/. - c.1902C>T r.(?) p.(Phe634=)
-?/. - c.1957+5dup r.spl? p.?
-?/. - c.2034A>G r.(?) p.(Glu678=)
+/. 10 c.2035T>A r.(?) p.(Ser679Thr)
-/. - c.2082-9T>C r.(=) p.(=)
?/. - c.2092C>T r.(?) p.(Arg698Trp)
?/. - c.2261A>G r.(?) p.(Lys754Arg)
-?/. - c.2294A>G r.(?) p.(Gln765Arg)
?/. - c.2294A>G r.(?) p.(Gln765Arg)
?/. - c.2294A>G r.(?) p.(Gln765Arg)
-/. - c.2367T>C r.(?) p.(Asp789=)
?/. - c.2372+6G>A r.(?) p.?
?/. - c.2456A>G r.(?) p.(His819Arg)
+/. 14 c.2459G>A r.(?) p.(Arg820His)
+/. 14 c.2459G>A r.(?) p.(Arg820His)
+/. 14 c.2459G>A r.(?) p.(Arg820His)
+/. 14 c.2459G>A r.(?) p.(Arg820His)
+/. 14 c.2459G>A r.(?) p.(Arg820His)
+/. 14 c.2459G>A r.(?) p.(Arg820His)
+/. 14 c.2459G>A r.(?) p.(Arg820His)
+/. 14 c.2459G>A r.(?) p.(Arg820His)
+?/. 14 c.2459G>A r.(?) p.(Arg820His)
-?/. - c.2523A>G r.(?) p.(Glu841=)
-/. - c.2523A>G r.(?) p.(Glu841=)
?/. - c.2544+4A>G r.spl p.(?)
?/. - c.2624T>C r.(?) p.(Leu875Pro)
?/. - c.2659C>T r.(?) p.(Arg887Ter)
-/. - c.2670T>C r.(?) p.(His890=)
-/. - c.2670T>C r.(?) p.(His890=)
-?/. - c.2680T>G r.(?) p.(Ser894Ala)
?/. 15i c.2699-8T>C r.(spl?) p.(?)
-/. - c.2699-8T>C r.(=) p.(=)
-?/. - c.2699-8T>C r.(=) p.(=)
?/. - c.2708G>A r.(?) p.(Arg903Gln)
?/. - c.2708G>A r.(?) p.(Arg903Gln)
?/. - c.2764C>A r.(?) p.(Pro922Thr)
?/. - c.2764C>A r.(?) p.(Pro922Thr)
?/. - c.2769A>G r.(?) p.(Pro923=)
-/. - c.2874C>T r.(?) p.(Arg958=)
?/. - c.2894C>T r.(?) p.(Pro965Leu)
-/. - c.2895G>A r.(?) p.(Pro965=)
?/. - c.2939A>C r.(?) p.(Glu980Ala)
-/. - c.2955A>G r.(?) p.(Arg985=)
+?/. - c.3027T>C r.(?) p.(Asp1009=)
?/. - c.3046C>T r.(?) p.(Gln1016Ter)
-/. - c.3060T>A r.(?) p.(Leu1020=)
?/. - c.3117-8C>T r.spl? p.(?)
-/. - c.3117-8C>T r.(=) p.(=)
+?/. 20 c.3136delA r.(?) p.(Thr1047Hisfs*31)
+/. - c.3139del r.(?) p.(Thr1047HisfsTer31)
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