Transcript #00005079 (NM_001271.3, CHD2 gene)

Transcript name transcript variant 1
Gene name CHD2 (chromodomain helicase DNA binding protein 2)
Chromosome 15
Transcript - NCBI ID NM_001271.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_001262.3
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

277 entries on 3 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.-367G>C r.(?) p.(=)
-?/. - c.-72+12A>G r.(=) p.(=)
-?/. - c.-71-104T>G r.(=) p.(=)
+/. - c.? r.? p.?
-?/. - c.25C>A r.(?) p.(Gln9Lys)
+?/. - c.59C>A r.(?) p.(Ser20*)
-?/. - c.62+3534A>G r.(=) p.(=)
-?/. - c.62+3644G>C r.(=) p.(=)
-?/. - c.62+3672A>G r.(=) p.(=)
+/. - c.106C>T r.(?) p.(Gln36Ter)
?/. - c.110C>T r.(?) p.(Ser37Leu)
./. - c.149G>A r.(?) p.(Gly50Asp)
-?/. - c.180T>G r.(?) p.(Ser60=)
?/. - c.185G>A r.(?) p.(Ser62Asn)
-?/. - c.239C>T r.(?) p.(Pro80Leu)
-?/. - c.239C>T r.(?) p.(Pro80Leu)
-?/. - c.239C>T r.(?) p.(Pro80Leu)
?/. - c.239C>T r.(?) p.(Pro80Leu)
-?/. - c.295-154A>T r.(=) p.(=)
-?/. - c.295-20G>A r.(=) p.(=)
+?/. - c.335C>G r.(?) p.(Ser112*)
?/. - c.340C>T r.(?) p.(Arg114Ter)
?/. - c.359C>T r.(?) p.(Ser120Leu)
+/. - c.361C>T r.(?) p.(Arg121*)
-?/. - c.382-179T>C r.(=) p.(=)
?/. - c.382del r.(?) p.(Ala128GlnfsTer18)
-?/. - c.443+223T>G r.(=) p.(=)
-?/. - c.444-2219G>C r.(=) p.(=)
-/. - c.444-237dup r.(=) p.(=)
-?/. - c.444-4A>C r.spl? p.?
+/. - c.532A>T r.(?) p.(Arg178*)
-?/. - c.551+116C>A r.(=) p.(=)
?/. - c.568C>T r.(?) p.(Arg190Cys)
-?/. - c.595C>T r.(?) p.(Arg199Cys)
-?/. - c.608A>G r.(?) p.(Lys203Arg)
-?/. - c.608A>G r.(?) p.(Lys203Arg)
-?/. - c.608A>G r.(?) p.(Lys203Arg)
-?/. - c.692+116C>G r.(=) p.(=)
-?/. - c.693-125G>T r.(=) p.(=)
-/. - c.693-122C>G r.(=) p.(=)
-?/. - c.693-20C>T r.(=) p.(=)
?/. - c.754G>A r.(?) p.(Gly252Arg)
?/. - c.767del r.(?) p.(Gln256Argfs*12)
?/. - c.826G>A r.(?) p.(Ala276Thr)
-?/. - c.826+27A>T r.(=) p.(=)
-?/. - c.826+115T>C r.(=) p.(=)
-/. - c.827-193dup r.(=) p.(=)
-?/. - c.827-146G>C r.(=) p.(=)
?/. - c.922C>T r.(?) p.(Leu308Phe)
?/. - c.922C>T r.(?) p.(Leu308Phe)
?/. - c.944C>G r.(?) p.(Ser315Cys)
-?/. - c.960A>T r.(?) p.(Thr320=)
?/. - c.983A>G r.(?) p.(Gln328Arg)
-?/. - c.1038C>T r.(?) p.(Asp346=)
+?/. - c.1052+1G>T r.spl? p.?
-?/. - c.1053-96A>G r.(=) p.(=)
-?/. - c.1053-46C>T r.(=) p.(=)
-?/. - c.1091A>G r.(?) p.(Asn364Ser)
+?/. - c.1153+1G>A r.spl? p.?
-?/. - c.1153+163G>A r.(=) p.(=)
-?/. - c.1154-197C>T r.(=) p.(=)
-?/. - c.1154-113del r.(=) p.(=)
-?/. - c.1154-110T>C r.(=) p.(=)
-?/. - c.1199-20A>T r.(=) p.(=)
-?/. - c.1214C>T r.(?) p.(Pro405Leu)
-?/. - c.1215G>A r.(?) p.(Pro405=)
?/. - c.1226A>G r.(?) p.(Asn409Ser)
-?/. - c.1274G>C r.(?) p.(Cys425Ser)
?/. - c.1274G>C r.(?) p.(Cys425Ser)
?/. - c.1274G>C r.(?) p.(Cys425Ser)
?/. - c.1372T>A r.(?) p.(Cys458Ser)
?/. - c.1377G>A r.(?) p.(Lys459=)
-?/. - c.1377+4T>C r.spl? p.?
-?/. - c.1377+151A>T r.(=) p.(=)
-?/. - c.1378-96T>G r.(=) p.(=)
-?/. - c.1378-5T>C r.spl? p.?
+/. - c.1396C>T r.(?) p.(Arg466*)
+/. - c.(1431_1432del) r.(?) p.(Arg1644Lysfs*22)
+/. - c.1453C>T r.(?) p.(Arg485*)
+/. - c.(1471_1472insT) r.(?) p.(Gly491Valfs*13)
+?/. - c.1486G>C r.(?) p.(Ala496Pro)
-?/. - c.1502+145A>G r.(=) p.(=)
-?/. - c.1502+156A>G r.(=) p.(=)
?/. - c.1618G>A r.(?) p.(Val540Ile)
+/. - c.1642T>C r.(?) p.(Trp548Arg)
+/. - c.1642T>M r.(?) p.(Trp548Arg)
+?/. - c.1644G>A r.(?) p.(Trp548*)
+/. - c.1645C>T r.(?) p.(Gln549*)
+/. - c.1693A>G r.(?) p.(Ile565Val)
?/. 14 c.1709G>A r.(?) p.(Ser570Asn)
+/. - c.1719G>A r.(?) p.(Thr573=)
-?/. - c.1719+12A>G r.(=) p.(=)
-?/. - c.1719+116C>T r.(=) p.(=)
-?/. - c.1810-158A>G r.(=) p.(=)
-?/. - c.1810-3T>C r.spl? p.?
+/. - c.1854A>T r.(?) p.(Glu618Asp)
+?/. - c.1880_1883del r.(?) p.(Ser627Tyrfs*6)
./. - c.1942C>T r.(?) p.(Pro648Ser)
-?/. - c.2000+24A>G r.(=) p.(=)
-?/. - c.2000+117G>A r.(=) p.(=)
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