Transcript #00014829 (NM_001135659.1, NRXN1 gene)

Transcript name transcript variant alpha2
Gene name NRXN1 (neurexin 1)
Chromosome 2
Transcript - NCBI ID NM_001135659.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001129131.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/. - c.-10822984_*22548674dup - -
-?/. - c.-922+7A>C r.(=) p.(=)
-/. - c.-883T>C r.(?) p.(=)
-?/. - c.105C>A r.(?) p.(Gly35=)
-?/. - c.172C>T r.(?) p.(Leu58Phe)
-?/. - c.222C>T r.(?) p.(Gly74=)
?/. - c.302C>G r.(?) p.(Ala101Gly)
-?/. - c.321G>T r.(?) p.(Thr107=)
?/. - c.479C>T r.(?) p.(Pro160Leu)
-?/. - c.501C>G r.(?) p.(Leu167=)
-?/. - c.501C>G r.(?) p.(Leu167=)
-/. - c.511C>T r.(?) p.(Leu171=)
-?/. - c.521T>C r.(?) p.(Val174Ala)
?/. - c.616G>C r.(?) p.(Asp206His)
?/. - c.707T>A r.(?) p.(Val236Glu)
-?/. - c.732C>T r.(?) p.(Asp244=)
?/. - c.739C>G r.(?) p.(Arg247Gly)
-?/. - c.772+9C>T r.(=) p.(=)
-?/. - c.780A>T r.(?) p.(Lys260Asn)
-?/. - c.790C>A r.(?) p.(Gln264Lys)
-?/. - c.790C>A r.(?) p.(Gln264Lys)
-?/. - c.818A>G r.(?) p.(Asp273Gly)
+/. - c.868_869del r.(?) p.(Glu290LysfsTer18)
+?/. - c.868_869del r.(?) p.(Glu290LysfsTer18)
-/. - c.890-794T>A r.(=) p.(=)
-/. - c.890-214A>G r.(=) p.(=)
+/. 5i_18i c.(919+1_920-1)_(3484+1_3485- 1)del r.? p.?
?/. - c.931+2636C>A r.(=) p.(=)
-/. - c.931+23184_931+23187del r.(=) p.(=)
-/. - c.932-7504A>C r.(=) p.(=)
-?/. - c.960A>G r.(?) p.(=)
-/. - c.963A>G r.(?) p.(Gly321=)
-?/. - c.1149C>G r.(?) p.(Ala383=)
-?/. - c.1149C>G r.(?) p.(Ala383=)
-/. - c.1234-168A>G r.(=) p.(=)
-?/. - c.1278+5A>T r.spl? p.?
-?/. - c.1278+5A>T r.spl? p.?
-?/. - c.1371A>G r.(?) p.(Gly457=)
-?/. - c.1405C>T r.(?) p.(Pro469Ser)
-?/. - c.1405C>T r.(?) p.(Pro469Ser)
?/. - c.1405C>T r.(?) p.(Pro469Ser)
-?/. - c.1485T>C r.(?) p.(Leu495=)
-?/. - c.1695A>G r.(?) p.(Arg565=)
-?/. - c.1695A>G r.(?) p.(Arg565=)
?/. - c.1873C>T r.(?) p.(Arg625Trp)
-/. - c.1879+108T>C r.(=) p.(=)
-?/. - c.1880-16C>T r.(=) p.(=)
-?/. - c.1899G>A r.(?) p.(Thr633=)
-?/. - c.2065A>G r.(?) p.(Ile689Val)
-?/. - c.2065A>G r.(?) p.(Ile689Val)
-?/. - c.2242C>A r.(?) p.(Leu748Ile)
-?/. - c.2277G>A r.(?) p.(Leu759=)
-?/. - c.2457G>C r.(?) p.(Thr819=)
?/. - c.2459T>A r.(?) p.(Val820Asp)
-/. - c.2467+55dup r.(=) p.(=)
-?/. - c.2505C>G r.(?) p.(Pro835=)
./. - c.2557C>T r.(?) p.(Arg853Cys)
-?/. - c.2627C>T r.(?) p.(Ala876Val)
?/. - c.2653C>T r.(?) p.(His885Tyr)
?/. - c.2653C>T r.(?) p.(His885Tyr)
?/. - c.2687G>A r.(?) p.(Arg896Gln)
?/. - c.2858C>T r.(?) p.(Ser953Leu)
-?/. - c.2999+20A>G r.(=) p.(=)
-/. - c.2999+73A>G r.(=) p.(=)
-?/. - c.3165C>T r.(?) p.(Ala1055=)
-?/. - c.3249A>G r.(?) p.(Val1083=)
-?/. - c.3249A>G r.(?) p.(Val1083=)
-?/. - c.3249A>G r.(?) p.(Val1083=)
-?/. - c.3321C>T r.(?) p.(Ser1107=)
-?/. - c.3348C>A r.(?) p.(Ile1116=)
-?/. - c.3353G>C r.(?) p.(Arg1118Thr)
?/. - c.3353G>C r.(?) p.(Arg1118Thr)
-/. - c.3365-942del r.(=) p.(=)
-/. - c.3369C>T r.(?) p.(Pro1123=)
?/. - c.3395G>T r.(?) p.(Cys1132Phe)
-/. - c.3484+20T>C r.(=) p.(=)
-/. - c.3485-110446C>A r.(=) p.(=)
?/. - c.3485-109939C>T r.(=) p.(=)
?/. - c.3485-109939C>T r.(=) p.(=)
?/. - c.3485-109928G>A r.(=) p.(=)
-/. - c.3485-109909_3485-109901del r.(=) p.(=)
?/. - c.3485-109906_3485-109901dup r.(=) p.(=)
-?/. - c.3485-109906_3485-109901dup r.(=) p.(=)
?/. - c.3485-109903_3485-109901del r.(=) p.(=)
?/. - c.3485-109891G>A r.(?) p.(=)
-?/. - c.3485-109709A>G r.(=) p.(=)
-/. - c.3666+28979C>T r.(=) p.(=)
-?/. - c.3750G>A r.(?) p.(Gly1250=)
-?/. - c.3838+9G>A r.(=) p.(=)
-?/. - c.4053A>G r.(?) p.(Ala1351=)
-?/. - c.4053A>G r.(?) p.(Ala1351=)
-?/. - c.4227G>A r.(?) p.(Pro1409=)
-/. - c.4248+34204T>G r.(=) p.(=)
-/. - c.4249-30181T>C r.(=) p.(=)
-?/. - c.4287C>G r.(?) p.(Pro1429=)
-?/. - c.4374A>G r.(?) p.(Pro1458=)
-?/. - c.4437C>T r.(?) p.(Ala1479=)
-?/. - c.4512T>C r.(?) p.(His1504=)
-?/. - c.4548A>G r.(?) p.(Ala1516=)
-?/. - c.4593G>A r.(?) p.(Ala1531=)
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