Transcript #00006136

Transcript name forkhead-associated (FHA) phosphopeptide binding domain 1
Gene name FHAD1 (forkhead-associated (FHA) phosphopeptide binding domain 1)
Chromosome 1
Transcript - NCBI ID NM_052929.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_443161.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

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

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/? c.-14-4G>A r.spl? p.?
?/? c.94-37del r.(=) p.(=)
?/? c.300G>A r.(=) p.(=)
?/? c.381C>T r.(=) p.(=)
?/? c.396T>C r.(=) p.(=)
?/? c.493C>T r.(?) p.(Arg165Trp)
?/? c.528C>T r.(=) p.(=)
?/? c.538G>A r.(?) p.(Asp180Asn)
?/? c.556G>A r.(?) p.(Val186Ile)
?/? c.569-34G>A r.(=) p.(=)
?/? c.603A>G r.(=) p.(=)
?/? c.610G>A r.(?) p.(Glu204Lys)
?/? c.613G>T r.(?) p.(Gly205Trp)
?/? c.657G>A r.(=) p.(=)
?/? c.678+44_678+48del r.(=) p.(=)
?/? c.754G>A r.(?) p.(Val252Ile)
?/? c.802G>A r.(?) p.(Val268Met)
?/? c.822C>T r.(=) p.(=)
?/? c.833_835del r.(?) p.(Lys279del)
?/? c.888G>C r.(?) p.(Gln296His)
?/? c.915+19G>A r.(=) p.(=)
?/? c.915+46C>T r.(=) p.(=)
?/? c.916-41G>A r.(=) p.(=)
?/? c.943A>C r.(?) p.(Lys315Gln)
?/? c.970C>T r.(?) p.(Arg324Trp)
?/? c.1039+39G>A r.(=) p.(=)
?/? c.1040-2A>G r.spl? p.?
?/? c.1068A>G r.(?) p.(Ile356Met)
?/? c.1116C>T r.(=) p.(=)
?/? c.1170+18C>T r.(=) p.(=)
?/? c.1171-35G>A r.(=) p.(=)
?/? c.1205A>T r.(?) p.(Asp402Val)
?/? c.1209T>C r.(=) p.(=)
?/? c.1249_1251del r.(?) p.(Leu417del)
?/? c.1260C>T r.(=) p.(=)
?/? c.1260+1G>A r.spl? p.?
?/? c.1366-36A>G r.(=) p.(=)
?/? c.1366-32G>A r.(=) p.(=)
?/? c.1473+5_1473+6insCATGT r.spl? p.?
?/? c.1473+7A>G r.(=) p.(=)
?/? c.1474-52A>G r.(=) p.(=)
?/? c.1474C>G r.(?) p.(Leu492Val)
?/? c.1482C>T r.(=) p.(=)
?/? c.1520C>T r.(?) p.(Ala507Val)
?/? c.1548C>T r.(=) p.(=)
?/? c.1557+11C>T r.(=) p.(=)
?/? c.1558-35_1558-34del r.(=) p.(=)
?/? c.1558-35_1558-34dup r.(=) p.(=)
?/? c.1558-34del r.(=) p.(=)
?/? c.1558-34dup r.(=) p.(=)
?/? c.1668C>T r.(=) p.(=)
?/? c.1671G>C r.(?) p.(Glu557Asp)
?/? c.1677C>T r.(=) p.(=)
?/? c.1692G>A r.(=) p.(=)
?/? c.1695G>A r.(=) p.(=)
?/? c.1710+2_1710+3insGGCC r.spl? p.?
?/? c.1710+13T>G r.(=) p.(=)
?/? c.1710+16G>A r.(=) p.(=)
?/? c.1813G>A r.(?) p.(Val605Met)
?/? c.1834G>A r.(?) p.(Ala612Thr)
?/? c.1871G>A r.(?) p.(Arg624Gln)
?/? c.1951G>A r.(?) p.(Gly651Arg)
?/? c.1992A>G r.(=) p.(=)
?/? c.1994G>A r.(?) p.(Arg665Gln)
?/? c.2047G>A r.(?) p.(Gly683Arg)
?/? c.2059G>A r.(?) p.(Gly687Ser)
?/? c.2135T>C r.(?) p.(Met712Thr)
?/? c.2173-10G>A r.(=) p.(=)
?/? c.2181G>A r.(=) p.(=)
?/? c.2242G>A r.(?) p.(Val748Ile)
?/? c.2280+5G>A r.spl? p.?
?/? c.2280+37C>T r.(=) p.(=)
?/? c.2317G>A r.(?) p.(Ala773Thr)
?/? c.2337G>A r.(=) p.(=)
?/? c.2389-12A>G r.(=) p.(=)
?/? c.2409G>A r.(=) p.(=)
?/? c.2419C>T r.(?) p.(Arg807Cys)
?/? c.2420G>A r.(?) p.(Arg807His)
?/? c.2496+9C>T r.(=) p.(=)
?/? c.2496+23G>T r.(=) p.(=)
?/? c.2496+25C>T r.(=) p.(=)
?/? c.2497-31C>G r.(=) p.(=)
?/? c.2550C>T r.(=) p.(=)
?/? c.2551G>A r.(?) p.(Ala851Thr)
?/? c.2560A>G r.(?) p.(Met854Val)
?/? c.2662A>G r.(?) p.(Thr888Ala)
?/? c.2670+24G>A r.(=) p.(=)
?/? c.2671-48G>A r.(=) p.(=)
?/? c.2684A>G r.(?) p.(Glu895Gly)
?/? c.2687G>A r.(?) p.(Arg896Gln)
?/? c.2749G>A r.(?) p.(Gly917Arg)
?/? c.2756A>G r.(?) p.(Glu919Gly)
?/? c.2839A>T r.(?) p.(Thr947Ser)
?/? c.2866G>A r.(?) p.(Glu956Lys)
?/? c.2867A>G r.(?) p.(Glu956Gly)
?/? c.2891A>G r.(?) p.(Asp964Gly)
?/? c.2896+9G>A r.(=) p.(=)
?/? c.2897-17A>G r.(=) p.(=)
?/? c.2915C>T r.(?) p.(Pro972Leu)
?/? c.2931G>A r.(=) p.(=)
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