Transcript #00021402 (NM_015896.2, ZMYND10 gene)

Transcript name zinc finger, MYND-type containing 10
Gene name ZMYND10 (zinc finger, MYND-type containing 10)
Chromosome 3
Transcript - NCBI ID NM_015896.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_056980.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

86 entries on 1 page. Showing entries 1 - 86.
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Affects function     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/? c.-1T>C r.(=) p.(=)
?/? c.24G>A r.(=) p.(=)
?/? c.47T>G r.(?) p.(Val16Gly)
?/? c.59G>A r.(?) p.(Arg20His)
?/? c.92+50G>A r.(=) p.(=)
?/? c.93-26G>A r.(=) p.(=)
?/? c.131T>C r.(?) p.(Met44Thr)
?/? c.155T>G r.(?) p.(Val52Gly)
?/? c.193C>T r.(?) p.(His65Tyr)
?/? c.202-14C>T r.(=) p.(=)
?/? c.229G>A r.(?) p.(Ala77Thr)
?/? c.318+3G>A r.spl? p.?
?/? c.319-36C>G r.(=) p.(=)
?/? c.319-22T>C r.(=) p.(=)
?/? c.319-13C>T r.(=) p.(=)
?/? c.319-9A>G r.(=) p.(=)
?/? c.319-6T>C r.(=) p.(=)
?/? c.334T>A r.(?) p.(Ser112Thr)
?/? c.344A>G r.(?) p.(Asn115Ser)
?/? c.355A>T r.(?) p.(Thr119Ser)
?/? c.372+21A>G r.(=) p.(=)
?/? c.372+29C>T r.(=) p.(=)
?/? c.373-53G>C r.(=) p.(=)
?/? c.373-14C>T r.(=) p.(=)
?/? c.373-11_373-9del r.(=) p.(=)
?/? c.420T>C r.(=) p.(=)
?/? c.427C>A r.(?) p.(Arg143Ser)
?/? c.470C>A r.(?) p.(Pro157His)
?/? c.477G>A r.(=) p.(=)
?/? c.478G>A r.(?) p.(Gly160Arg)
?/? c.480G>A r.(=) p.(=)
?/? c.485G>A r.(?) p.(Gly162Glu)
?/? c.490C>T r.(?) p.(Gln164*)
?/? c.510+1G>A r.spl? p.?
?/? c.510+8G>C r.(=) p.(=)
?/? c.510+13T>C r.(=) p.(=)
?/? c.510+42G>A r.(=) p.(=)
?/? c.511-43G>A r.(=) p.(=)
?/? c.511-24C>T r.(=) p.(=)
?/? c.511-15T>G r.(=) p.(=)
?/? c.564C>G r.(=) p.(=)
?/? c.595G>A r.(?) p.(Asp199Asn)
?/? c.599+11C>T r.(=) p.(=)
?/? c.599+48C>T r.(=) p.(=)
?/? c.599+49G>A r.(=) p.(=)
?/? c.600-32A>G r.(=) p.(=)
?/? c.623G>A r.(?) p.(Arg208His)
?/? c.637C>T r.(?) p.(His213Tyr)
?/? c.642C>G r.(?) p.(Asn214Lys)
?/? c.656T>A r.(?) p.(Leu219Gln)
?/? c.687C>A r.(?) p.(Ser229Arg)
?/? c.689G>A r.(?) p.(Arg230Gln)
?/? c.701-51A>T r.(=) p.(=)
?/? c.701-18G>A r.(=) p.(=)
?/? c.727C>T r.(?) p.(Arg243Cys)
?/? c.728G>A r.(?) p.(Arg243His)
?/? c.765G>C r.(=) p.(=)
?/? c.794C>T r.(?) p.(Ala265Val)
?/? c.832C>T r.(?) p.(Arg278Cys)
?/? c.873+4A>T r.spl? p.?
?/? c.873+15G>A r.(=) p.(=)
?/? c.873+32C>T r.(=) p.(=)
?/? c.873+41G>A r.(=) p.(=)
?/? c.970C>A r.(?) p.(Pro324Thr)
?/? c.999+7A>T r.(=) p.(=)
?/? c.1000-13_1000-12del r.(=) p.(=)
?/? c.1019G>A r.(?) p.(Arg340Gln)
?/? c.1061A>T r.(?) p.(Lys354Met)
?/? c.1073A>G r.(?) p.(Gln358Arg)
?/? c.1105C>T r.(?) p.(Arg369Trp)
?/? c.1115C>A r.(?) p.(Ala372Glu)
?/? c.1116G>A r.(=) p.(=)
?/? c.1121+2T>C r.spl? p.?
?/? c.1121+34G>C r.(=) p.(=)
?/? c.1137C>T r.(=) p.(=)
?/? c.1171C>T r.(?) p.(Arg391Trp)
?/? c.1178G>A r.(?) p.(Arg393His)
?/? c.1229A>G r.(?) p.(Asn410Ser)
?/? c.1247+25C>T r.(=) p.(=)
?/? c.1248-33G>T r.(=) p.(=)
?/? c.1248-30T>C r.(=) p.(=)
?/? c.1248-22C>G r.(=) p.(=)
?/? c.1248-1G>T r.spl? p.?
?/? c.1291G>A r.(?) p.(Val431Ile)
?/? c.*25C>T r.(=) p.(=)
?/? c.*39G>A r.(=) p.(=)
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