Transcript #00022384 (NM_001080421.2, UNC13A gene)

Transcript name unc-13 homolog A (C. elegans)
Gene name UNC13A (unc-13 homolog A (C. elegans))
Chromosome 19
Transcript - NCBI ID NM_001080421.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_001073890.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

63 entries on 1 page. Showing entries 1 - 63.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.116G>A r.(?) p.(Arg39Gln)
+/. - c.154G>A r.(?) p.(Glu52Lys)
?/. - c.164G>A r.(?) p.(Arg55His)
?/. - c.169G>C r.(?) p.(Asp57His)
?/. - c.182C>T r.(?) p.(Thr61Met)
-?/. - c.182C>T r.(?) p.(Thr61Met)
?/. - c.451A>C r.(?) p.(Met151Leu)
-?/. - c.457G>T r.(?) p.(Asp153Tyr)
-/. - c.474G>C r.(?) p.(Ser158=)
-/. - c.474G>C r.(?) p.(Ser158=)
?/. - c.691C>T r.(?) p.(Pro231Ser)
?/. - c.728T>A r.(?) p.(Met243Lys)
-?/. - c.771C>G r.(?) p.(=)
?/. - c.785G>C r.(?) p.(Arg262Pro)
-?/. - c.861G>T r.(?) p.(=)
?/. - c.892C>T r.(?) p.(Arg298Trp)
?/. - c.941C>T r.(?) p.(Ser314Leu)
-?/. - c.1049_1051del r.(?) p.(Glu350del)
-/. - c.1075G>A r.(?) p.(Ala359Thr)
-/. - c.1075G>A r.(?) p.(Ala359Thr)
?/. - c.1196C>G r.(?) p.(Ala399Gly)
?/. - c.1602C>G r.(?) p.(Asn534Lys)
-/. - c.1767C>G r.(?) p.(Val589=)
?/. - c.2036G>T r.(?) p.(Ser679Ile)
-?/. - c.2044+3G>A r.spl? p.?
-?/. - c.2223C>T r.(?) p.(=)
?/. - c.2303C>A r.(?) p.(Thr768Lys)
+?/. - c.2423G>A r.(?) p.(Gly808Asp)
?/. - c.2423G>T r.(?) p.(Gly808Val)
+?/. - c.2441C>T r.(?) p.(Pro814Leu)
+?/. - c.2441C>T r.(?) p.(Pro814Leu)
+?/. - c.2441C>T r.(?) p.(Pro814Leu)
-?/. - c.2622C>T r.(?) p.(=)
-/. - c.3101T>C r.(?) p.(Leu1034Pro)
?/. - c.3103C>T r.(?) p.(Pro1035Ser)
-?/. - c.3108G>A r.(?) p.(Glu1036=)
-/. - c.3108G>A r.(?) p.(Glu1036=)
?/. - c.3386C>T r.(?) p.(Thr1129Met)
-/. - c.3397G>T r.(?) p.(Ala1133Ser)
?/. - c.3401T>C r.(?) p.(Phe1134Ser)
?/. - c.3428+1G>A r.spl? p.?
-?/. - c.3552A>G r.(?) p.(Leu1184=)
-?/. - c.3573T>C r.(?) p.(=)
-/. - c.3576T>C r.(?) p.(Val1192=)
-/. - c.3687C>T r.(?) p.(Leu1229=)
-?/. - c.3687C>T r.(?) p.(Leu1229=)
?/. - c.3697G>A r.(?) p.(Ala1233Thr)
?/. - c.3767_3772del r.(?) p.(Met1256_Asn1257del)
-/. - c.3831+14G>A r.(=) p.(=)
-?/. - c.3950A>G r.(?) p.(Lys1317Arg)
-/. - c.4029C>T r.(?) p.(Asp1343=)
-?/. - c.4029C>T r.(?) p.(Asp1343=)
-/. - c.4073+7T>C r.(=) p.(=)
-?/. - c.4197+7C>T r.(=) p.(=)
-/. - c.4197+7C>T r.(=) p.(=)
?/. - c.4243-8C>T r.(=) p.(=)
?/. - c.4272C>T r.(?) p.(Asp1424=)
-/. - c.4273-16A>C r.(=) p.(=)
?/. - c.4396C>G r.(?) p.(Leu1466Val)
-/. - c.4497G>A r.(?) p.(Ser1499=)
-/. - c.4558+9A>G r.(=) p.(=)
?/. - c.4855G>A r.(?) p.(Val1619Met)
-/. - c.5079C>A r.(?) p.(Ser1693=)
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