Transcript #00010236 (NM_003024.2, ITSN1 gene)

Transcript name transcript variant 1
Gene name ITSN1 (intersectin 1 (SH3 domain protein))
Chromosome 21
Transcript - NCBI ID NM_003024.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_003015.2
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

57 entries on 1 page. Showing entries 1 - 57.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+?/. - c.186-2A>G r.spl p.?
?/. - c.201G>A r.(?) p.(Met67Ile)
?/. - c.457G>A r.(?) p.(Ala153Thr)
?/. - c.469C>G r.(?) p.(Pro157Ala)
-?/. - c.724+19T>G r.(=) p.(=)
-?/. - c.739A>G r.(?) p.(Thr247Ala)
?/. - c.758G>C r.(?) p.(Ser253Thr)
?/. - c.786A>G r.(?) p.(Ile262Met)
-?/. - c.789-5A>G r.spl? p.?
?/. - c.853C>A r.(?) p.(Leu285Ile)
?/. - c.887C>T r.(?) p.(Pro296Leu)
-?/. - c.927-10G>A r.(=) p.(=)
?/. - c.1017del r.(?) p.(Gln339Hisfs*4)
?/. - c.1274A>C r.(?) p.(Glu425Ala)
+?/. - c.1357C>T r.(?) p.(Arg453*)
-/. - c.1566C>T r.(?) p.(Ala522=)
?/. - c.1615G>A r.(?) p.(Gly539Arg)
-?/. - c.1646A>G r.(?) p.(Asn549Ser)
-?/. - c.1702C>T r.(?) p.(Leu568Phe)
?/. - c.1703T>G r.(?) p.(Leu568Arg)
?/. - c.1885C>T r.(?) p.(Arg629*)
-?/. - c.1952+10C>T r.(=) p.(=)
-?/. - c.1962G>A r.(?) p.(Gln654=)
?/. - c.2080G>A r.(?) p.(Glu694Lys)
?/. - c.2212G>A r.(?) p.(Glu738Lys)
-?/. - c.2319+14_2319+17del r.(=) p.(=)
-/. - c.2641G>A r.(?) p.(Val881Ile)
+?/. - c.2842_2843del r.(?) p.(Met948ValfsTer41)
+?/. 24 c.2974C>T r.(?) p.(Arg992*)
?/. - c.3125C>G r.(?) p.(Thr1042Arg)
?/. - c.3310C>T r.(?) p.(Arg1104*)
?/. - c.3371A>G r.(?) p.(Gln1124Arg)
-?/. - c.3469+7A>C r.(=) p.(=)
?/. - c.3485G>A r.(?) p.(Gly1162Glu)
?/. - c.3502G>A r.(?) p.(Ala1168Thr)
?/. - c.3541A>G r.(?) p.(Ile1181Val)
-?/. - c.3700A>G r.(?) p.(Thr1234Ala)
?/. - c.3707G>T r.(?) p.(Arg1236Ile)
?/. - c.3790C>T r.(?) p.(Gln1264*)
-?/. - c.3807G>A r.(?) p.(Glu1269=)
?/. - c.3947G>C r.(?) p.(Gly1316Ala)
?/. - c.4018G>A r.(?) p.(Ala1340Thr)
-?/. - c.4146A>G r.(?) p.(Val1382=)
-?/. - c.4227C>T r.(?) p.(Ala1409=)
?/. - c.4274G>A r.(?) p.(Arg1425Gln)
-?/. - c.4314C>A r.(?) p.(Ala1438=)
-?/. - c.4332C>G r.(?) p.(Gly1444=)
?/. - c.4379C>T r.(?) p.(Pro1460Leu)
-?/. - c.4555-8C>A r.(=) p.(=)
?/. - c.4666A>G r.(?) p.(Ile1556Val)
-?/. - c.4676+12C>T r.(=) p.(=)
-?/. - c.4676+13G>A r.(=) p.(=)
?/. - c.4720A>G r.(?) p.(Ile1574Val)
-?/. - c.4809T>C r.(?) p.(=)
-?/. - c.4884G>A r.(?) p.(Gln1628=)
?/. - c.5162C>T r.(?) p.(Pro1721Leu)
-?/. - c.5163G>A r.(?) p.(Pro1721=)
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