Transcript #00005080 (NM_001005273.2, CHD3 gene)

Transcript name transcript variant 1
Gene name CHD3 (chromodomain helicase DNA binding protein 3)
Chromosome 17
Transcript - NCBI ID NM_001005273.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_001005273.1
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

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+/. _1_40_ c.-150_*1172[0] r.0 p.0
+/. _1_40_ c.-150_*1172[0] r.(=) p.(=)
-?/. - c.-4158_-4153dup r.(?) p.(=)
-?/. - c.-4082C>A r.(?) p.(=)
-?/. - c.-4032G>C r.(?) p.(=)
?/. - c.-4016G>A r.(?) p.(=)
-?/. - c.-3981C>T r.(?) p.(=)
-?/. - c.-3962C>T r.(?) p.(=)
-?/. - c.-3961_-3953del r.(?) p.(=)
-/. - c.-3955_-3953dup r.(?) p.(=)
-/. - c.-3955_-3953dup r.(?) p.(=)
?/. - c.-3950_-3949insCCC r.(?) p.(=)
-?/. - c.-3944C>T r.(?) p.(=)
?/. - c.-3943_-3935del r.(?) p.(=)
?/. - c.81T>A r.(?) p.(Cys27*)
?/. - c.125C>T r.(?) p.(Pro42Leu)
?/. - c.175G>A r.(?) p.(Glu59Lys)
-?/. - c.241C>G r.(?) p.(Arg81Gly)
-?/. - c.241C>T r.(?) p.(Arg81*)
?/. - c.308G>A r.(?) p.(Arg103Gln)
?/. - c.722C>T r.(?) p.(Ala241Val)
-?/. - c.793+4G>A r.spl? p.?
?/. - c.812G>A r.(?) p.(Arg271Gln)
-?/. - c.842G>A r.(?) p.(Arg281His)
?/. - c.924G>A r.(?) p.(=)
?/. - c.977T>C r.(?) p.(Leu326Pro)
?/. - c.1099G>A r.(?) p.(Gly367Arg)
?/. - c.1301A>G r.(?) p.(Glu434Gly)
?/. - c.1325_1327del r.(?) p.(Glu442del)
+/. - c.1369G>T r.(?) p.(Glu457*)
?/. - c.1373A>T r.(?) p.(Tyr458Phe)
?/. - c.1378C>T r.(?) p.(Arg460Cys)
+/. - c.1384del r.(?) p.(Cys462Alafs*22)
?/. - c.1430C>T r.(?) p.(Ser477Phe)
-?/. - c.1503+3G>A r.spl? p.?
+/. - c.1618dup r.(?) p.(Arg540Profs*47)
+/. - c.1706A>G r.(?) p.(Gln569Arg)
+?/. - c.1706A>G r.(?) p.(Gln569Arg)
?/. - c.1748G>A r.(?) p.(Arg583Gln)
?/. - c.1888T>C r.(?) p.(Trp630Arg)
?/. - c.1900C>T r.(?) p.(His634Tyr)
?/. - c.2075C>T r.(?) p.(Pro692Leu)
?/. - c.2084C>T r.(?) p.(Pro695Leu)
-?/. - c.2193C>T r.(?) p.(Ala731=)
?/. - c.2260G>A r.(?) p.(Gly754Ser)
+?/. 14 c.2288T>C r.(?) p.(Met763Thr)
-?/. - c.2327A>G r.(?) p.(Tyr776Cys)
-?/. - c.2344-3C>T r.spl? p.?
?/. - c.2422G>T r.(?) p.(Ala808Ser)
+?/. 16 c.2653G>A r.(?) p.(Ala885Thr)
+/. - c.2657A>G r.(?) p.(His886Arg)
+/. - c.2657A>G r.(?) p.(His886Arg)
+/. - c.2745G>T r.(?) p.(Leu915Phe)
+/. - c.2749A>T r.(?) p.(Asn917Tyr)
+/. - c.2761G>A r.(?) p.(Glu921Lys)
+?/. - c.2771A>G r.(?) p.(His924Arg)
+/. - c.2831T>A r.(?) p.(Phe944Tyr)
+/. - c.2842T>C r.(?) p.(Ser948Pro)
+?/. - c.2842T>C r.(?) p.(Ser948Pro)
?/. - c.2882G>A r.(?) p.(Gly961Glu)
+/. - c.2882G>A r.(?) p.(Gly961Glu)
+/. - c.2896C>T r.(?) p.(Arg966Trp)
+/. - c.2896C>T r.(?) p.(Arg966Trp)
+/. - c.2896C>T r.(?) p.(Arg966Trp)
+/. - c.2897G>A r.(?) p.(Arg966Gln)
+/. - c.2897G>C r.(?) p.(Arg966Pro)
+?/. - c.2897G>T r.(?) p.(Arg966Leu)
+/. - c.2905A>G r.(?) p.(Lys969Glu)
+/. - c.2953C>T r.(?) p.(Arg985Trp)
+/. - c.2953C>T r.(?) p.(Arg985Trp)
+/. - c.2953C>T r.(?) p.(Arg985Trp)
+/. - c.2953C>T r.(?) p.(Arg985Trp)
+/. - c.2953C>T r.(?) p.(Arg985Trp)
+/. - c.2953C>T r.(?) p.(Arg985Trp)
+/. - c.2953C>T r.(?) p.(Arg985Trp)
+/. - c.2954G>A r.(?) p.(Arg985Gln)
+/. - c.2954G>A r.(?) p.(Arg985Gln)
?/. - c.3005G>C r.(?) p.(Arg1002Pro)
+?/. - c.3061A>T r.(?) p.(Ile1021Phe)
?/. - c.3171G>C r.(?) p.(Lys1057Asn)
+?/. - c.3206T>C r.(?) p.(Leu1069Pro)
?/. - c.3217A>C r.(?) p.(Lys1073Gln)
+/. - c.3239T>A r.(?) p.(Leu1080His)
+?/. - c.3319G>A r.(?) p.(Asp1107Asn)
+/. - c.3325_3327del r.(?) p.(Gly1109del)
+/. - c.3357_3358delinsTC r.(?) p.(Asp1120His)
+/. - c.3362G>C r.(?) p.(Arg1121Pro)
+/. - c.3407C>T r.(?) p.(Thr1136Ile)
?/. - c.3409C>T r.(?) p.(Arg1137Ter)
+/. - c.3472T>C r.(?) p.(Trp1158Arg)
?/. - c.3473G>A r.(?) p.(Trp1158Ter)
+/. - c.3477C>A r.(?) p.(Asn1159Lys)
+/. - c.3482A>G r.(?) p.(His1161Arg)
+/. - c.3482A>G r.(?) p.(His1161Arg)
+?/. - c.3488A>T r.(?) p.(Asp1163Val)
+/. - c.3505C>T r.(?) p.(Arg1169Trp)
+/. - c.3505C>T r.(?) p.(Arg1169Trp)
+/. - c.3505C>T r.(?) p.(Arg1169Trp)
+/. - c.3505C>T r.(?) p.(Arg1169Trp)
+/. - c.3505C>T r.(?) p.(Arg1169Trp)
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