Transcript #00024138 (NM_032504.1, UNC80 gene)

Transcript name transcript variant 1
Gene name UNC80 (unc-80 homolog (C. elegans))
Chromosome 2
Transcript - NCBI ID NM_032504.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_115893.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2016-05-26 09:45:43 +02:00 (CEST)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.92+7G>A r.(=) p.(=)
+/. - c.151C>T r.(?) p.(Arg51*)
?/. - c.400G>A r.(?) p.(Gly134Ser)
+/. - c.409C>T r.(?) p.(Arg137Ter)
-?/. - c.448C>A r.(?) p.(His150Asn)
+?/. 4 c.565G>A r.(?) p.(Val189Met)
+?/. 4 c.565G>A r.(?) p.(Val189Met)
-?/. - c.601-5C>A r.spl? p.?
+/. - c.798+1G>T r.spl p.?
-?/. - c.857T>C r.(?) p.(Ile286Thr)
+/. - c.871C>T r.(?) p.(Arg291Ter)
?/. 8 c.1020G>T r.(?) p.(Gln340His)
?/. - c.1020G>T r.(?) p.(Gln340His)
?/. 8 c.1021C>T r.(?) p.(Pro341Ser)
?/. - c.1021C>T r.(?) p.(Pro341Ser)
+?/. 8 c.1078C>T r.(?) p.(Arg360*)
+?/. - c.1078C>T r.(?) p.(Arg360*)
?/. - c.1078C>T r.(?) p.(Arg360Ter)
-?/. - c.1147A>G r.(?) p.(Ser383Gly)
?/. - c.1313T>C r.(?) p.(Leu438Pro)
?/. - c.1564C>T r.(?) p.(Arg522Trp)
-?/. - c.1620C>G r.(?) p.(Ser540=)
-?/. - c.1620C>G r.(?) p.(Ser540=)
-?/. - c.1693+365C>T r.(=) p.(=)
?/. - c.1763A>C r.(?) p.(Tyr588Ser)
-?/. - c.1806G>C r.(?) p.(Gln602His)
?/. - c.1806G>C r.(?) p.(Gln602His)
?/. - c.1806G>C r.(?) p.(Gln602His)
?/. - c.2012G>A r.(?) p.(Arg671His)
+?/. 13 c.2033del r.(?) p.(Asn678Thrfs*15)
+?/. 13 c.2033del r.(?) p.(Asn678Thrfs*15)
?/. - c.2213G>A r.(?) p.(Gly738Glu)
-?/. - c.2267A>T r.(?) p.(Asp756Val)
?/. - c.2273G>C r.(?) p.(Gly758Ala)
?/. - c.2286_2294del r.(?) p.(Gly764_Gly766del)
-?/. - c.2382C>T r.(?) p.(Ile794=)
-?/. - c.2471G>A r.(?) p.(Arg824Gln)
?/. - c.2534C>T r.(?) p.(Thr845Ile)
-?/. - c.2700C>T r.(?) p.(Ile900=)
?/. - c.3043G>A r.(?) p.(Asp1015Asn)
?/. - c.3169C>T r.(?) p.(His1057Tyr)
+/. - c.3205C>T r.(?) p.(Arg1069*)
?/. - c.3256+3A>G r.spl? p.?
-?/. - c.3356G>C r.(?) p.(Ser1119Thr)
?/. - c.3356G>C r.(?) p.(Ser1119Thr)
?/. - c.3356G>C r.(?) p.(Ser1119Thr)
-?/. - c.3434A>C r.(?) p.(Glu1145Ala)
?/. - c.3473T>G r.(?) p.(Phe1158Cys)
+?/. 23 c.3719G>A r.(?) p.(Trp1240*)
+/. - c.3793C>T r.(?) p.(Arg1265*)
+/. - c.3793C>T r.(?) p.(Arg1265*)
?/. - c.3793C>T r.(?) p.(Arg1265Ter)
+?/. 23 c.3793C>T r.(?) p.(Arg1265*)
+?/. 23 c.3793C>T r.(?) p.(Arg1265*)
+?/. 23 c.3793C>T r.(?) p.(Arg1265*)
-?/. - c.3842G>C r.(?) p.(Gly1281Ala)
-?/. - c.3846C>T r.(?) p.(Asp1282=)
-?/. - c.3932C>T r.(?) p.(Thr1311Ile)
-?/. - c.3983-10C>G r.(=) p.(=)
-/. - c.3983-4C>A r.spl? p.?
-?/. - c.4117-5T>C r.spl? p.?
-?/. - c.4374G>A r.(?) p.(Ser1458=)
?/. - c.4435T>C r.(?) p.(Tyr1479His)
?/. - c.4442A>G r.(?) p.(His1481Arg)
?/. - c.4687C>T r.(?) p.(Leu1563Phe)
?/. - c.4838T>C r.(?) p.(Met1613Thr)
+?/. 31 c.4926_4937del r.(?) p.(Asn1643_Leu1646del)
+?/. 31 c.4963C>T r.(?) p.(Arg1655Cys)
+/. - c.5093G>A r.(?) p.(Trp1698Ter)
+?/. 32 c.5098C>T r.(?) p.(Pro1700Ser)
-/. - c.5229G>C r.(?) p.(Lys1743Asn)
?/. - c.5263G>A r.(?) p.(Ala1755Thr)
-?/. - c.5301A>G r.(?) p.(Thr1767=)
?/. - c.5761C>T r.(?) p.(Pro1921Ser)
+/. - c.(?_5986)_(6717+199_?)del r.? p.?
-?/. - c.6100C>T r.(?) p.(Pro2034Ser)
?/. - c.6278G>A r.(?) p.(Arg2093Gln)
-?/. - c.6449-6T>C r.(=) p.(=)
?/. - c.6559A>G r.(?) p.(Met2187Val)
?/. - c.6785A>G r.(?) p.(Tyr2262Cys)
-/. - c.7020A>G r.(?) p.(Thr2340=)
-?/. - c.7117T>A r.(?) p.(Leu2373Ile)
-?/. - c.7272C>T r.(?) p.(Ala2424=)
+/. - c.7607G>C r.(?) p.(Arg2536Thr)
+?/. 50 c.7607G>C r.(?) p.(Arg2536Thr)
?/. - c.7684C>T r.(?) p.(Arg2562Cys)
+?/. - c.7697A>C r.(?) p.(Glu2566Ala)
+?/. 51 c.7757T>A r.(?) p.(Leu2586*)
+/. 51 c.7757T>A r.(?) p.(Leu2586*)
?/. - c.8126G>A r.(?) p.(Gly2709Glu)
+?/. 55 c.8216_8228del r.(?) p.(Leu2739GlnfsTer22)
?/. - c.8254C>T r.(?) p.(Arg2752Trp)
?/. - c.8263A>G r.(?) p.(Ser2755Gly)
?/. - c.8330C>T r.(?) p.(Ala2777Val)
-?/. - c.8337A>G r.(?) p.(Lys2779=)
+?/. 55 c.8385C>G r.(?) p.(Tyr2795*)
?/. - c.8391G>A r.(?) p.(Ala2797=)
-?/. - c.8427C>T r.(?) p.(Leu2809=)
+?/. - c.8574+2T>G r.spl? p.?
?/. - c.8626A>G r.(?) p.(Ile2876Val)
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