Transcript #00016391 (NM_017514.3, PLXNA3 gene)

Transcript name plexin A3
Gene name PLXNA3 (plexin A3)
Chromosome X
Transcript - NCBI ID NM_017514.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_059984.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
./. - c.-120955_*1021401dup - -
./. - c.-116388_*160080dup r.0? p.0?
-?/. - c.39C>T r.(?) p.(Ala13=)
-?/. - c.56G>A r.(?) p.(Gly19Asp)
-?/. - c.71G>A r.(?) p.(Arg24His)
-?/. - c.78C>T r.(?) p.(Phe26=)
-?/. - c.79G>A r.(?) p.(Val27Met)
-?/. - c.138C>T r.(?) p.(Phe46=)
-?/. - c.172C>T r.(?) p.(Pro58Ser)
?/. - c.196C>T r.(?) p.(His66Tyr)
+?/. - c.196C>T r.(?) p.(His66Tyr)
?/. - c.202A>G r.(?) p.(Thr68Ala)
-?/. - c.210C>T r.(?) p.(Pro70=)
-?/. - c.213C>T r.(?) p.(Val71=)
-?/. - c.222C>T r.(?) p.(Asn74=)
-?/. - c.252C>T r.(?) p.(Arg84=)
-?/. - c.272C>G r.(?) p.(Ala91Gly)
-?/. - c.315G>A r.(?) p.(Ala105=)
-?/. - c.320G>A r.(?) p.(Arg107His)
-?/. - c.336C>T r.(?) p.(Cys112=)
-?/. - c.371G>A r.(?) p.(Arg124His)
-?/. - c.409C>T r.(?) p.(Arg137Cys)
?/. - c.409C>T r.(?) p.(Arg137Cys)
-?/. - c.444C>T r.(?) p.(Pro148=)
-?/. - c.513C>T r.(?) p.(Val171=)
?/. - c.673T>C r.(?) p.(Tyr225His)
-?/. - c.685G>A r.(?) p.(Gly229Ser)
-?/. - c.720G>A r.(?) p.(Thr240=)
?/. - c.734C>T r.(?) p.(Thr245Ile)
-?/. - c.825C>T r.(?) p.(Tyr275=)
?/. - c.836C>G r.(?) p.(Pro279Arg)
?/. - c.869G>A r.(?) p.(Arg290His)
-?/. - c.933G>A r.(?) p.(Pro311=)
-?/. - c.933G>A r.(=) p.(=)
-?/. - c.958A>G r.(?) p.(Ile320Val)
?/. - c.982C>T r.(?) p.(Arg328Trp)
-?/. - c.984G>A r.(?) p.(Arg328=)
?/. - c.997C>T r.(?) p.(Arg333Trp)
?/. - c.998G>A r.(?) p.(Arg333Gln)
-?/. - c.998G>A r.(?) p.(Arg333Gln)
-?/. - c.1039G>A r.(?) p.(Ala347Thr)
-?/. - c.1098C>T r.(?) p.(Pro366=)
-?/. - c.1138A>G r.(?) p.(Met380Val)
-?/. - c.1167G>A r.(?) p.(Leu389=)
-?/. - c.1167G>A r.(=) p.(=)
-?/. - c.1234G>A r.(?) p.(Asp412Asn)
-/. - c.1237G>A r.(?) p.(Gly413Ser)
-?/. - c.1254C>T r.(?) p.(Ala418=)
-/. - c.1255G>A r.(?) p.(Ala419Thr)
?/. - c.1259A>G r.(?) p.(Tyr420Cys)
-?/. - c.1268G>A r.(?) p.(Arg423His)
-?/. - c.1284C>T r.(?) p.(Val428=)
-?/. - c.1296G>A r.(?) p.(Thr432=)
-?/. - c.1298G>A r.(?) p.(Arg433His)
?/. - c.1298G>A r.(?) p.(Arg433His)
-?/. - c.1298G>A r.(?) p.(Arg433His)
?/. - c.1314G>C r.(?) p.(Lys438Asn)
?/. - c.1322G>A r.(?) p.(Arg441Gln)
?/. - c.1322G>A r.(?) p.(Arg441Gln)
-?/. - c.1362C>G r.(?) p.(Val454=)
-?/. - c.1461G>A r.(?) p.(Pro487=)
-?/. - c.1468A>T r.(?) p.(Thr490Ser)
-?/. - c.1510G>A r.(?) p.(Gly504Arg)
-?/. - c.1512G>C r.(?) p.(Gly504=)
-?/. - c.1547+13del r.(=) p.(=)
?/. - c.1557C>A r.(?) p.(Arg519=)
?/. - c.1627C>T r.(?) p.(Arg543Trp)
-?/. - c.1628G>A r.(?) p.(Arg543Gln)
?/. - c.1628G>A r.(?) p.(Arg543Gln)
-?/. - c.1639A>G r.(?) p.(Asn547Asp)
-?/. - c.1656G>A r.(?) p.(Thr552=)
-?/. - c.1695G>A r.(?) p.(Val565=)
?/. - c.1729G>A r.(?) p.(Glu577Lys)
-?/. - c.1752G>A r.(?) p.(Ala584=)
-?/. - c.1767C>T r.(?) p.(Ser589=)
-?/. - c.1773A>T r.(?) p.(Glu591Asp)
?/. - c.1828+7G>A r.(=) p.(=)
-?/. - c.1918G>A r.(?) p.(Val640Ile)
-?/. - c.1926G>C r.(?) p.(Gln642His)
?/. - c.1958C>T r.(?) p.(Pro653Leu)
-/. - c.1958C>T r.(?) p.(Pro653Leu)
?/. - c.1996C>T r.(?) p.(Arg666Cys)
-?/. - c.2002C>G r.(?) p.(His668Asp)
?/. - c.2170C>T r.(?) p.(Arg724Trp)
-?/. - c.2171G>A r.(?) p.(Arg724Gln)
?/. - c.2192G>A r.(?) p.(Arg731Gln)
-?/. - c.2289C>T r.(=) p.(=)
?/. - c.2363C>T r.(?) p.(Ala788Val)
-?/. - c.2448G>A r.(?) p.(Leu816=)
-?/. - c.2469G>A r.(?) p.(Pro823=)
?/. - c.2589C>G r.(?) p.(Asp863Glu)
-?/. - c.2620C>T r.(?) p.(Leu874=)
-?/. - c.2721G>C r.(?) p.(Pro907=)
-?/. - c.2751C>T r.(?) p.(Asp917=)
-?/. - c.2807C>T r.(?) p.(Thr936Met)
-?/. - c.2808G>A r.(?) p.(Thr936=)
?/. - c.2855G>A r.(?) p.(Arg952Gln)
-?/. - c.2855G>A r.(?) p.(Arg952Gln)
-?/. - c.2900C>G r.(?) p.(Thr967Arg)
-?/. - c.2901A>G r.(=) p.(=)
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