Transcript #00024066 (NM_005393.2, PLXNB3 gene)

Transcript name transcript variant 1
Gene name PLXNB3 (plexin B3)
Chromosome X
Transcript - NCBI ID NM_005393.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_005384.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2015-10-18 16:58:25 +02:00 (CEST)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
./. - c.-319019_*565412dup r.0? p.0?
+/. _1_2i c.-33583_46-378del r.0? p.0?
?/. - c.46-587C>T r.(=) p.(=)
-?/. - c.46-565G>A r.(=) p.(=)
-?/. - c.68C>A r.(?) p.(Pro23His)
?/. - c.91C>A r.(?) p.(Leu31Met)
-?/. - c.238G>A r.(?) p.(Glu80Lys)
+?/. - c.331C>T r.(?) p.(Gln111*)
-?/. - c.366G>A r.(?) p.(Val122=)
-?/. - c.376G>A r.(?) p.(Ala126Thr)
-?/. - c.396C>T r.(?) p.(Cys132=)
-?/. - c.406C>T r.(?) p.(Arg136Trp)
-?/. - c.648C>T r.(?) p.(Ser216=)
?/. - c.662G>A r.(?) p.(Arg221His)
?/. - c.672G>A r.(?) p.(Val224=)
?/. - c.703G>A r.(?) p.(Val235Ile)
-?/. - c.828C>T r.(?) p.(Tyr276=)
?/. - c.872C>A r.(?) p.(Ala291Asp)
?/. - c.938C>T r.(?) p.(Ala313Val)
-?/. - c.1015C>T r.(?) p.(Arg339Trp)
-?/. - c.1027G>A r.(?) p.(Gly343Ser)
-?/. - c.1029C>T r.(?) p.(Gly343=)
?/. - c.1057G>A r.(?) p.(Val353Ile)
-?/. - c.1057G>A r.(?) p.(Val353Ile)
-?/. - c.1062G>A r.(?) p.(Thr354=)
-?/. - c.1095C>T r.(?) p.(Pro365=)
?/. - c.1151C>A r.(?) p.(Pro384His)
+?/. - c.1154T>A r.(?) p.(Leu385Gln)
?/. - c.1198G>A r.(?) p.(Val400Met)
-?/. - c.1209C>T r.(=) p.(=)
-?/. - c.1358G>A r.(?) p.(Ser453Asn)
?/. 6 c.1466C>T r.(?) p.(Pro489Leu)
./. - c.1496+35C>T r.(=) p.(=)
./. - c.1496+35C>T r.(=) p.(=)
?/. - c.1519G>A r.(?) p.(Gly507Arg)
-?/. - c.1715A>G r.(?) p.(His572Arg)
-?/. - c.1776T>C r.(=) p.(=)
-?/. 9 c.1792G>A r.(?) p.(Val598Ile)
-?/. 9 c.1792G>A r.(?) p.(Val598Ile)
?/. - c.1895C>T r.(?) p.(Pro632Leu)
-?/. - c.1901G>A r.(?) p.(Arg634His)
-?/. - c.1912G>A r.(?) p.(Gly638Ser)
-?/. - c.1962C>T r.(?) p.(Tyr654=)
-?/. - c.1988G>C r.(?) p.(Arg663Thr)
-?/. - c.1991C>T r.(?) p.(Thr664Ile)
+?/. - c.1991_2009delinsGGT r.(?) p.(Thr664Argfs*115)
-?/. - c.2008G>A r.(?) p.(Glu670Lys)
-?/. - c.2113G>A r.(?) p.(Val705Met)
?/. - c.2156A>G r.(?) p.(His719Arg)
+?/. - c.2173C>T r.(?) p.(Pro725Ser)
?/. - c.2185C>T r.(?) p.(Arg729Trp)
-?/. - c.2208G>A r.(=) p.(=)
-?/. - c.2221G>A r.(?) p.(Asp741Asn)
?/. - c.2221G>A r.(?) p.(Asp741Asn)
-?/. - c.2307G>C r.(?) p.(Gln769His)
-?/. - c.2307G>C r.(?) p.(Gln769His)
?/. - c.2365G>A r.(?) p.(Ala789Thr)
-?/. - c.2378C>T r.(?) p.(Pro793Leu)
-?/. - c.2474C>T r.(?) p.(Pro825Leu)
-?/. 14i c.2518-44C>T r.(?) p.(=)
-?/. 14i c.2518-44C>T r.(?) p.(=)
-?/. - c.2585G>T r.(?) p.(Arg862Leu)
?/. - c.2627G>A r.(?) p.(Arg876Gln)
./. - c.2670-43C>G r.(=) p.(=)
./. - c.2670-43C>G r.(=) p.(=)
?/. - c.2729T>C r.(?) p.(Ile910Thr)
./. - c.2775+66G>A r.(=) p.(=)
./. - c.2775+66G>A r.(=) p.(=)
./. - c.2775+257G>C r.(=) p.(=)
./. - c.2775+257G>C r.(=) p.(=)
./. - c.2906+45C>G r.(=) p.(=)
./. - c.2906+45C>G r.(=) p.(=)
./. - c.2907-24G>C r.(=) p.(=)
./. - c.2907-24G>C r.(=) p.(=)
-?/. - c.2942G>A r.(?) p.(Arg981His)
-?/. - c.2995C>A r.(?) p.(His999Asn)
+?/. - c.3005G>A r.(?) p.(Arg1002His)
-?/. - c.3028C>T r.(?) p.(Arg1010Cys)
?/. - c.3079C>T r.(?) p.(Arg1027Trp)
-?/. - c.3080G>A r.(?) p.(Arg1027Gln)
+?/. - c.3140T>C r.(?) p.(Leu1047Pro)
-?/. - c.3279+3G>A r.spl? p.?
-?/. - c.3279+8C>T r.(=) p.(=)
-?/. - c.3361C>A r.(?) p.(Arg1121=)
?/. - c.3362G>A r.(?) p.(Arg1121Gln)
?/. - c.3446G>A r.(?) p.(Arg1149His)
?/. - c.3452C>T r.(?) p.(Ala1151Val)
./. - c.3468G>C r.(?) p.(Glu1156Asp)
./. - c.3468G>C r.(?) p.(Glu1156Asp)
+?/. - c.3519+1G>T r.spl p.?
./. - c.3520-26A>G r.(=) p.(=)
./. - c.3520-26A>G r.(=) p.(=)
-?/. - c.3738G>A r.(?) p.(Pro1246=)
+?/. - c.3986C>G r.(?) p.(Pro1329Arg)
-?/. - c.4039G>A r.(?) p.(Gly1347Ser)
-?/. - c.4062T>C r.(?) p.(Pro1354=)
-?/. - c.4080C>T r.(?) p.(Asp1360=)
-?/. - c.4113G>A r.(=) p.(=)
-?/. - c.4141C>T r.(?) p.(Leu1381Phe)
-?/. - c.4184G>A r.(?) p.(Ser1395Asn)
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