Transcript #00025819 (NM_024596.3, MCPH1 gene)

Transcript name transcript variant 1
Gene name MCPH1 (microcephalin 1)
Chromosome 8
Transcript - NCBI ID NM_024596.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_078872.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2023-03-13 19:42:40 +01:00 (CET)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.-10G>C r.(?) p.(=)
-?/. - c.7G>T r.(?) p.(Ala3Ser)
-/. - c.23-26G>A r.(=) p.(=)
-/. - c.23-15A>G r.(=) p.(=)
?/. - c.58G>A r.(?) p.(Gly20Arg)
?/. - c.89C>T r.(?) p.(Thr30Ile)
?/. - c.128T>C r.(?) p.(Phe43Ser)
+/. - c.179G>A r.(?) p.(Trp60Ter)
?/. - c.182A>G r.(?) p.(Asp61Gly)
-/. - c.228G>T r.(?) p.(Val76=)
-/. - c.228G>T r.(?) p.(Val76=)
-/. - c.228G>T r.(?) p.(Val76=)
-?/. - c.295C>T r.(?) p.(His99Tyr)
-?/. - c.305G>C r.(?) p.(Ser102Thr)
+/. - c.427dup r.(?) p.(Thr143AsnfsTer5)
-?/. - c.433C>T r.(?) p.(Leu145=)
?/. - c.445G>A r.(?) p.(Val149Ile)
-?/. - c.477A>T r.(?) p.(Ser159=)
-/. - c.513= r.(=) p.(Ser171=)
-/. - c.513= r.(=) p.(Ser171=)
+?/. - c.580+1G>A r.spl? p.?
-/. - c.581-29C>A r.(=) p.(=)
?/. - c.610A>G r.(?) p.(Asn204Asp)
+/. - c.625_626del r.(?) p.(Leu209Valfs*2)
-/. - c.634G>A r.(?) p.(Ala212Thr)
-/. - c.634G>A r.(?) p.(Ala212Thr)
-?/. - c.634G>A r.(?) p.(Ala212Thr)
-/. - c.647T>C r.(?) p.(Ile216Thr)
-?/. - c.696C>T r.(?) p.(His232=)
-?/. - c.783T>A r.(?) p.(Asp261Glu)
-?/. - c.790A>G r.(?) p.(Ile264Val)
-/. - c.863C>A r.(?) p.(Pro288His)
-/. - c.863C>A r.(?) p.(Pro288His)
-?/. - c.863C>A r.(?) p.(Pro288His)
?/. - c.869A>G r.(?) p.(Lys290Arg)
-?/. - c.908A>G r.(?) p.(Gln303Arg)
-/. - c.911G>T r.(?) p.(Arg304Ile)
-/. - c.911G>T r.(?) p.(Arg304Ile)
-/. - c.911G>T r.(?) p.(Arg304Ile)
-/. - c.940G>C r.(?) p.(Asp314His)
-/. - c.940G>C r.(?) p.(Asp314His)
-/. - c.940G>C r.(?) p.(Asp314His)
-/. - c.989A>G r.(?) p.(Tyr330Cys)
-?/. - c.1052G>T r.(?) p.(Ser351Ile)
-?/. - c.1061T>C r.(?) p.(Val354Ala)
-?/. - c.1065G>T r.(?) p.(Lys355Asn)
-?/. - c.1148C>G r.(?) p.(Pro383Arg)
-/. - c.1175A>G r.(?) p.(Asp392Gly)
-/. - c.1175A>G r.(?) p.(Asp392Gly)
-/. - c.1175A>G r.(?) p.(Asp392Gly)
-?/. - c.1188C>A r.(?) p.(His396Gln)
-?/. - c.1226A>T r.(?) p.(Glu409Val)
-?/. - c.1236T>C r.(?) p.(Tyr412=)
-?/. - c.1349A>C r.(?) p.(Lys450Thr)
-?/. - c.1351G>A r.(?) p.(Glu451Lys)
-?/. - c.1369G>A r.(?) p.(Glu457Lys)
-?/. - c.1390G>A r.(?) p.(Val464Ile)
-?/. - c.1403C>A r.(?) p.(Thr468Asn)
-/. - c.1428C>T r.(?) p.(Phe476=)
-/. - c.1428C>T r.(?) p.(Phe476=)
-?/. - c.1430C>T r.(?) p.(Thr477Ile)
-?/. - c.1463G>A r.(?) p.(Gly488Glu)
-?/. - c.1477C>T r.(?) p.(Arg493Cys)
-?/. - c.1493G>C r.(?) p.(Cys498Ser)
-?/. - c.1551C>T r.(?) p.(Asp517=)
-?/. - c.1589A>T r.(?) p.(Glu530Val)
?/. - c.1679G>T r.(?) p.(Ser560Ile)
-/. - c.1719C>T r.(?) p.(Ser573=)
-/. - c.1719C>T r.(?) p.(Ser573=)
-?/. - c.1728C>T r.(?) p.(Gly576=)
-/. - c.1728C>T r.(?) p.(Gly576=)
-?/. - c.1779G>C r.(?) p.(Glu593Asp)
-?/. - c.1781C>T r.(?) p.(Thr594Met)
-/. - c.1782G>A r.(?) p.(Thr594=)
-/. - c.1782G>A r.(?) p.(Thr594=)
?/. - c.1782G>A r.(=) p.(=)
-?/. - c.1785T>C r.(?) p.(Ser595=)
-?/. - c.1825+1G>C r.spl? p.?
?/. - c.1825+2956G>A r.(=) p.(=)
?/. - c.1958C>G r.(?) p.(Thr653Arg)
?/. - c.1987G>A r.(?) p.(Val663Ile)
-?/. - c.2023A>G r.(?) p.(Ile675Val)
-/. - c.2045C>A r.(?) p.(Thr682Asn)
-/. - c.2045C>A r.(?) p.(Thr682Asn)
?/. - c.2077C>T r.(?) p.(Arg693Cys)
?/. - c.2078G>A r.(?) p.(Arg693His)
?/. - c.2093T>G r.(?) p.(Leu698Arg)
?/. - c.2126C>T r.(?) p.(Ser709Phe)
+/. - c.2145G>A r.(?) p.(Trp715Ter)
?/. - c.2180C>T r.(?) p.(Pro727Leu)
?/. - c.2180C>T r.(?) p.(Pro727Leu)
?/. - c.2180C>T r.(?) p.(Pro727Leu)
?/. - c.2202C>A r.(?) p.(Phe734Leu)
?/. - c.2210C>G r.(?) p.(Ala737Gly)
?/. - c.2214+3203G>T r.(=) p.(=)
-/. - c.2214+13790C>G r.(=) p.(=)
-/. - c.2214+13841A>G r.(=) p.(=)
-/. - c.2214+13853A>G r.(=) p.(=)
-?/. - c.2214+14783C>T r.(=) p.(=)
-?/. - c.2214+19953A>T r.(=) p.(=)
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