Transcript #00002975 (NM_018489.2, ASH1L gene)

Transcript name ash1 (absent, small, or homeotic)-like (Drosophila)
Gene name ASH1L (ash1 (absent, small, or homeotic)-like (Drosophila))
Chromosome 1
Transcript - NCBI ID NM_018489.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_060959.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+/. - c.-480_*2399{0} r.0 p.0
+/. - c.-480_*2399{0} r.0 p.0
+/. - c.-480_*2399{0} r.0 p.0
+/. - c.-480_*2399{0} r.0 p.0
-?/. - c.-99-9271C>G r.(=) p.(=)
+?/. - c.-480_*2398{0} r.0 p.0
+/. _1_28_ c.-480_*2399{0} r.0 p.0
?/. - c.67C>T r.(?) p.(Pro23Ser)
-?/. - c.80G>A r.(?) p.(Ser27Asn)
+?/. - c.102G>C r.(?) p.(Lys34Asn)
+?/. - c.175G>A r.(?) p.(Glu59Lys)
+?/. - c.221C>T r.(?) p.(Ser74Leu)
+?/. - c.295C>A r.(?) p.(Pro99Thr)
-?/. - c.305A>C r.(?) p.(Asn102Thr)
-?/. - c.420+234T>A r.(=) p.(=)
+?/. - c.491G>A r.(?) p.(Arg164His)
+?/. - c.503A>T r.(?) p.(Gln168Leu)
+?/. - c.557C>T r.(?) p.(Ala186Val)
+?/. - c.581_582dup r.(?) p.(Thr195Leufs*11)
+?/. - c.588del r.(?) p.(Gly198Valfs*7)
?/. - c.593G>T r.(?) p.(Gly198Val)
-?/. - c.598C>T r.(?) p.(Arg200Trp)
+?/. - c.607G>A r.(?) p.(Asp203Asn)
-?/. - c.692A>G r.(?) p.(Lys231Arg)
?/. - c.773G>A r.(?) p.(Gly258Asp)
+?/. - c.902A>G r.(?) p.(Asn301Ser)
?/. - c.928A>G r.(?) p.(Thr310Ala)
?/. - c.1074G>T r.(?) p.(Lys358Asn)
?/. - c.1156G>A r.(?) p.(Asp386Asn)
?/. - c.1282G>A r.(?) p.(Ala428Thr)
?/. - c.1373A>G r.(?) p.(Asp458Gly)
?/. - c.1411C>T r.(?) p.(Arg471Trp)
-?/. - c.1451G>A r.(?) p.(Arg484Gln)
?/. - c.1460T>A r.(?) p.(Ile487Asn)
+?/. - c.1516_1517del r.(?) p.(Phe506LeufsTer4)
+?/. - c.1657A>G r.(?) p.(Ser553Gly)
+?/. - c.1690G>A r.(?) p.(Val564Ile)
-?/. - c.1743T>G r.(?) p.(Asn581Lys)
+?/. - c.1919A>G r.(?) p.(His640Arg)
?/. - c.2029A>G r.(?) p.(Ser677Gly)
+/. - c.2134dup r.(?) p.(Arg712Lysfs*10)
?/. - c.2170G>T r.(?) p.(Ala724Ser)
./. - c.2170G>T r.(?) p.(Ala724Ser)
+?/. - c.2186G>A r.(?) p.(Arg729Gln)
+?/. - c.2192C>G r.(?) p.(Pro731Arg)
+?/. - c.2254A>G r.(?) p.(Asn752Asp)
?/. - c.2321T>C r.(?) p.(Phe774Ser)
-?/. - c.2377T>G r.(?) p.(Leu793Val)
?/. - c.2394A>T r.(?) p.(Lys798Asn)
+/. - c.2422_2423delinsT r.(?) p.(Lys808Tyrfs*40)
+?/. - c.2473A>G r.(?) p.(Lys825Glu)
-?/. - c.2550T>G r.(?) p.(Pro850=)
?/. - c.2567C>G r.(?) p.(Ser856Cys)
?/. - c.2590_2592del r.(?) p.(Glu864del)
+?/. - c.2605C>T r.(?) p.(Gln869*)
?/. - c.2632A>G r.(?) p.(Lys878Glu)
+/. - c.2678dup r.(?) p.(Lys894*)
-?/. - c.2795G>A r.(?) p.(Ser932Asn)
?/. - c.2884C>T r.(?) p.(Leu962Phe)
+?/. - c.3028A>G r.(?) p.(Asn1010Asp)
+/. - c.3033del r.(?) p.(Val1014Cysfs*24)
+?/. - c.3033del r.(?) p.(Val1014Cysfs*24)
+?/. - c.3040G>A r.(?) p.(Val1014Met)
-?/. - c.3169A>C r.(?) p.(Thr1057Pro)
?/. - c.3224A>G r.(?) p.(Gln1075Arg)
?/. - c.3229G>A r.(?) p.(Ala1077Thr)
?/. - c.3269C>T r.(?) p.(Pro1090Leu)
-?/. - c.3319A>G r.(?) p.(Ile1107Val)
+?/. - c.3319A>G r.(?) p.(Ile1107Val)
+?/. - c.3319A>G r.(?) p.(Ile1107Val)
-?/. - c.3319A>G r.(?) p.(Ile1107Val)
-?/. - c.3319A>G r.(?) p.(Ile1107Val)
?/. - c.3341C>A r.(?) p.(Thr1114Asn)
+?/. - c.3445_3446del r.(?) p.(Leu1149Cysfs*27)
+?/. - c.3479G>A r.(?) p.(Arg1160Gln)
?/. - c.3490_3492del r.(?) p.(Pro1164del)
+?/. - c.3491C>T r.(?) p.(Pro1164Leu)
?/. - c.3503C>A r.(?) p.(Pro1168Gln)
-?/. - c.3594C>T r.(?) p.(Pro1198=)
+/. - c.3705del r.(?) p.(Glu1236Lysfs*6)
+?/. - c.3744_3745del r.(?) p.(His1248GlnfsTer5)
+?/. - c.3744_3745del r.(?) p.(His1248GlnfsTer5)
+?/. - c.3744_3745del r.(?) p.(His1248GlnfsTer5)
-?/. - c.3783C>T r.(?) p.(Ser1261=)
?/. - c.3823A>G r.(?) p.(Lys1275Glu)
-?/. - c.3856G>A r.(?) p.(Asp1286Asn)
?/. - c.3983A>G r.(?) p.(Tyr1328Cys)
?/. - c.3989A>G r.(?) p.(His1330Arg)
?/. - c.4036T>G r.(?) p.(Leu1346Val)
+?/. - c.4039_4043del r.(?) p.(Lys1347GlufsTer7)
+/. - c.4039_4043del r.(?) p.(Lys1347Glufs*7)
+/. - c.4048del r.(?) p.(Arg1350Glufs*7)
+?/. - c.4096A>G r.(?) p.(Met1366Val)
?/. - c.4112T>A r.(?) p.(Phe1371Tyr)
?/. - c.4343G>A r.(?) p.(Arg1448Gln)
?/. - c.4546C>T r.(?) p.(Arg1516Cys)
+?/. - c.4552A>G r.(?) p.(Arg1518Gly)
+?/. - c.4567G>A r.(?) p.(Ala1523Thr)
+?/. - c.4583A>G r.(?) p.(Tyr1528Cys)
-?/. - c.4589A>T r.(?) p.(His1530Leu)
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