Transcript #00006605 (NM_022552.4, DNMT3A gene)

Transcript name transcript variant 3
Gene name DNMT3A (DNA (cytosine-5-)-methyltransferase 3 alpha)
Chromosome 2
Transcript - NCBI ID NM_022552.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_072046.2
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

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/. - c.-781G>T r.(?) p.(=)
+/. _1_23_ c.0 r.0 p.0
?/. - c.56G>A r.(?) p.(Arg19Gln)
?/. - c.56G>A r.(?) p.(Arg19Gln)
-/. - c.72+10G>A r.(=) p.(=)
-?/. - c.72+10G>A r.(=) p.(=)
-?/. - c.75C>T r.(?) p.(=)
-?/. - c.76G>A r.(?) p.(Gly26Arg)
?/. - c.89A>C r.(?) p.(Glu30Ala)
-?/. - c.89A>C r.(?) p.(Glu30Ala)
-?/. - c.106G>A r.(?) p.(Glu36Lys)
-?/. - c.120G>A r.(?) p.(=)
-?/. - c.131C>T r.(?) p.(Thr44Met)
?/. - c.172C>G r.(?) p.(Pro58Ala)
-?/. - c.176C>T r.(?) p.(Pro59Leu)
-?/. - c.178-8A>G r.(=) p.(=)
-?/. - c.186C>T r.(?) p.(=)
-?/. - c.194C>T r.(?) p.(Thr65Met)
-?/. - c.209C>T r.(?) p.(Ala70Val)
?/. - c.337G>A r.(?) p.(Gly113Arg)
+?/. - c.427C>T r.(?) p.(Arg143*)
-?/. - c.448+45A>G r.(=) p.(=)
+?/. - c.541C>T r.(?) p.(Arg181Cys)
?/. - c.553A>G r.(?) p.(Met185Val)
-?/. - c.639+6G>A r.(=) p.(=)
-?/. - c.640-3791G>A r.(=) p.(=)
-?/. - c.640-1431C>T r.(=) p.(=)
-?/. - c.640-1403T>G r.(=) p.(=)
-?/. - c.759C>T r.(?) p.(=)
-?/. - c.801C>T r.(?) p.(Ser267=)
-?/. - c.801C>T r.(?) p.(Ser267=)
-?/. - c.801C>T r.(?) p.(Ser267=)
+?/. - c.855+1G>A r.(?) p.(?)
?/. - c.886G>A r.(?) p.(Val296Met)
+/. 8 c.889_891del r.(?) p.(Trp297del)
+/. - c.890G>A r.(?) p.(Trp297Ter)
+/. - c.901C>T r.(?) p.(Arg301Trp)
+?/. 8 c.919C>T r.(?) p.(Pro307Ser)
?/. - c.925del r.(?) p.(Arg309Alafs*7)
?/. - c.926G>A r.(?) p.(Arg309His)
+?/. - c.928A>T r.(?) p.(Ile310Phe)
+/. 8 c.929T>A r.(?) p.(Ile310Asn)
+/. 8 c.934_937dup r.(?) p.(Trp313Phefs*12)
+?/. 8 c.958C>T r.(?) p.(Arg320*)
?/. - c.971G>T r.(?) p.(Gly324Val)
+/. - c.980_983dup r.(?) p.(Met329Glyfs*15)
-?/. - c.993C>T r.(?) p.(=)
+?/. - c.1034del r.(?) p.(Met345Serfs*3)
-?/. - c.1055G>A r.(?) p.(Ser352Asn)
+?/. - c.1080_1082del r.(?) p.(Asn360del)
+?/. 8 c.1084C>T r.(?) p.(Gln362*)
+?/. 8 c.1094A>G r.(?) p.(Tyr365Cys)
+/. - c.1111del r.(?) p.(Glu371ArgfsTer36)
?/. - c.1138G>A r.(?) p.(Ala380Thr)
-?/. - c.1155G>A r.(?) p.(=)
-?/. - c.1170C>T r.(?) p.(Ser390=)
-?/. - c.1275A>C r.(?) p.(Pro425=)
?/. - c.1296C>G r.(?) p.(Tyr432Ter)
-?/. - c.1310C>T r.(?) p.(Thr437Met)
-?/. - c.1386G>A r.(?) p.(Ala462=)
-?/. - c.1430-13C>T r.(=) p.(=)
+/. 13 c.1481G>C r.(?) p.(Cys494Ser)
-?/. - c.1502A>G r.(?) p.(Asn501Ser)
-?/. - c.1502A>G r.(?) p.(Asn501Ser)
-?/. - c.1554+9A>G r.(=) p.(=)
-?/. - c.1555-13C>T r.(=) p.(=)
+?/. 14 c.1585G>A r.(?) p.(Asp529Asn)
-?/. - c.1587C>T r.(?) p.(=)
?/. - c.1594G>A r.(?) p.(Gly532Ser)
+/. 14 c.1594G>A r.(?) p.(Gly532Ser)
+?/. 14 c.1627G>A r.(1627g>a) p.(Gly543Ser)
+/. 14 c.1643T>A r.(?) p.(Met548Lys)
+?/. - c.1643T>C r.(?) p.(Met548Thr)
+/. 14 c.1645T>C r.(?) p.(Cys549Arg)
+?/. - c.1667+2T>G r.spl p.?
-?/. - c.1677C>T r.(?) p.(=)
+/. 15 c.1681G>T r.(?) p.(Glu561*)
?/. - c.1741T>C r.(?) p.(Trp581Arg)
+/. - c.1795G>T r.(?) p.(Glu599*)
+/. - c.1803G>A r.(?) p.(Trp601*)
+/. - c.1803G>A r.(?) p.(Trp601Ter)
?/. - c.1852-3T>G r.spl? p.?
+?/. - c.1904G>A r.(?) p.(Arg635Gln)
+?/. - c.1907T>C r.(?) p.(Val636Ala)
-?/. - c.1936+8G>A r.(=) p.(=)
+/. 19 c.1943T>C r.(?) p.(Leu648Pro)
?/. - c.1974_1975dup r.(?) p.(Arg659ProfsTer47)
+/. - c.1975dup r.(?) p.(Arg659Profs*9)
?/. - c.1976G>A r.(?) p.(Arg659His)
+?/. - c.2062C>T r.(?) p.(Arg688Cys)
+?/. - c.2063G>A r.(?) p.(Arg688His)
?/. - c.2063G>A r.(?) p.(Arg688His)
+/. - c.2074C>T r.(?) p.(Gln692Ter)
+/. 18 c.2099C>T r.(?) p.(Pro700Leu)
+/. - c.2141C>G r.(?) p.(Ser714Cys)
+?/. - c.2141C>G r.(?) p.(Ser714Cys)
-/. - c.2151C>T r.(?) p.(Asn717=)
-?/. - c.2151C>T r.(?) p.(Asn717=)
?/. - c.2158C>T r.(?) p.(Arg720Cys)
+/. - c.2171_2172del r.(?) p.(Tyr724*)
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