Transcript #00001074 (NM_006306.2, SMC1A gene)

Transcript name structural maintenance of chromosomes 1A
Gene name SMC1A (structural maintenance of chromosomes 1A)
Chromosome X
Transcript - NCBI ID NM_006306.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_006297.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2012-09-13 13:11:18 +02:00 (CEST)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
./. - c.-231639_109+108dup r.0 p.0
-?/. 1 c.-19C>T r.(=) p.(=)
-?/. 1 c.-19C>T r.(=) p.(=)
-/. - c.-19C>T r.(?) p.(=)
?/? 1 c.-19C>T r.(?) p.(=)
+?/+? 1 c.31A>T r.(?) p.(Asn11Tyr)
?/? 1 c.82A>C r.(?) p.Thr28Pro
+?/. - c.92T>C r.(?) p.(Ile31Thr)
-/. - c.109+104dup r.(=) p.(=)
-?/. 1i c.109+104dup r.(=) p.(=)
-?/. 1i c.109+104dup r.(=) p.(=)
-?/. - c.109+575A>C r.(=) p.(=)
-?/. - c.109+582A>C r.(=) p.(=)
+?/. 2 c.110G>T r.(?) p.(Gly37Val)
+/. 2 c.116C>G r.(?) p.(Ser39*)
+?/. 2 c.121C>T r.(?) p.(Leu41Phe)
+?/. 2 c.121C>T r.(?) p.(Leu41Phe)
+?/. 2 c.128A>T r.(?) p.(Asp43Val)
+?/. 2 c.140T>G r.(?) p.(Phe47Cys)
+/? 2 c.173_187del r.(?) p.(Val58_Arg62del)
+/+ 2 c.173_187del r.(?) p.(Val58_Arg62del)
+?/. 2 c.298G>C r.(?) p.(Gly100Arg)
-?/. - c.372G>C r.(?) p.(Leu124Phe)
-?/. - c.372G>C r.(?) p.(Leu124Phe)
+/? 3 c.397T>G r.(?) p.(Phe133Val)
-?/. - c.412-10C>T r.(=) p.(=)
+/+ 3 c.421G>A r.(?) p.(Glu141Lys)
?/. - c.494C>T r.(?) p.(Ala165Val)
+?/. - c.557A>G r.(?) p.(Tyr186Cys)
+?/. - c.563G>A r.(?) p.(Arg188His)
-?/. - c.579G>A r.(?) p.(=)
+?/. - c.586C>T r.(?) p.(Arg196Cys)
+?/. 4 c.586C>T r.(?) p.(Arg196Cys)
+/? 4 c.587G>A r.(?) p.(Arg196His)
+/+ 4 c.587G>A r.(?) p.(Arg196His)
+/+? 4 c.587G>A r.(?) p.(Arg196His)
?/. - c.598A>C r.(?) p.(Lys200Gln)
+?/. - c.607A>G r.(?) p.(Lys203Glu)
+/. 5 c.655del r.(?) p.(Ala219Leufs*45)
-?/. - c.699G>A r.(?) p.(=)
?/. - c.707A>G r.(?) p.(Glu236Gly)
-?/. - c.707A>G r.(?) p.(Glu236Gly)
+?/. - c.725T>C r.(?) p.(Leu242Pro)
?/. - c.751_753del r.(?) p.(Lys251del)
+?/. - c.784G>T r.(?) p.(Glu262*)
+?/. 5 c.802_804del r.(?) p.(Lys268del)
+/. 5 c.802_804del r.(?) p.(Lys268del)
+/+ 5 c.802_804del r.(?) p.(Lys268del)
+/+? 5 c.802_804del r.(?) p.(Lys268del)
-?/. - c.855-15C>T r.(=) p.(=)
-?/. - c.855-15C>T r.(=) p.(=)
+/+ 5 c.916_918del r.(?) p.(Ser306del)
+/. - c.1113+1G>A r.spl? p.?
+/. 7i c.1114-2A>G r.spl p.?
-?/. - c.1119G>A r.(?) p.(Lys373=)
+?/. - c.1141G>A r.(?) p.(Glu381Lys)
+/. - c.1150A>G r.(?) p.(Lys384Glu)
+?/+? 7 c.1169C>A r.(?) p.(Ala390Asp)
-?/. - c.1173G>A r.(?) p.(Gln391=)
+/+ 7 c.1192C>G r.(?) p.(Arg398Gly)
+/+ 7 c.1193G>A r.(?) p.(Arg398Gln)
?/. - c.1217G>A r.(?) p.(Arg406His)
?/. 7 c.1235G>A r.(?) p.(Arg412Gln)
-?/. - c.1254+4G>A r.spl? p.?
-?/. - c.1254+4G>A r.spl? p.?
-?/. - c.1254+11G>C r.(=) p.(=)
-/. - c.1254+62C>A r.(=) p.(=)
-?/. - c.1284T>G r.(?) p.(Ile428Met)
-?/. - c.1312C>T r.(?) p.(=)
-?/. - c.1323C>T r.(?) p.(Tyr441=)
?/. 8i c.1338-32C>A r.(spl?) p.(=)
?/. 8i c.1338-32C>A r.(=) p.(=)
?/. - c.1361A>G r.(?) p.(Lys454Arg)
+/. - c.1364T>C r.(?) p.(Leu455Pro)
+/? 9 c.1478A>C r.(?) p.(Glu493Ala)
+/? 9 c.1478A>C r.(?) p.Glu493Ala
+/? 9 c.1486C>T r.(?) p.(Arg496Cys)
+/? 9 c.1487G>A r.(?) p.(Arg496His)
+/? 9 c.1487G>A r.(?) p.(Arg496His)
+/? 9 c.1487G>A r.(?) p.(Arg496His)
+/. 9 c.1487G>A r.(?) p.(Arg496His)
+/? 9 c.1487G>A r.(?) p.(Arg496His)
+/? 9 c.1487G>A r.(?) p.(Arg496His)
+/? 9 c.1487G>A r.(?) p.(Arg496His)
+/? 9 c.1487G>A r.(?) p.Arg496His
-?/. - c.1545+4A>C r.spl? p.?
-?/. - c.1545+4A>C r.spl? p.?
-?/. - c.1545+4A>C r.spl? p.?
-?/. - c.1548C>T r.(?) p.(Tyr516=)
+/. - c.1576A>C r.(?) p.(Thr526Pro)
?/. - c.1678A>G r.(?) p.(Ile560Val)
-/. - c.1698G>A r.(?) p.(Glu566=)
-?/. - c.1767G>A r.(?) p.(Lys589=)
-?/. - c.1788T>C r.(?) p.(Asp596=)
-?/. - c.1863C>T r.(?) p.(Asn621=)
?/. - c.1904G>A r.(?) p.(Arg635His)
-?/. - c.1912-14C>T r.(=) p.(=)
+?/+? 12 c.1937T>C r.(?) p.(Phe646Ser)
+/+ 12 c.1951G>A r.(?) p.(Val651Met)
+?/+? 12 c.1955T>A r.(?) p.(Ile652Asn)
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