Transcript #00001179 (NM_152486.2, SAMD11 gene)

Transcript name sterile alpha motif domain containing 11
Gene name SAMD11 (sterile alpha motif domain containing 11)
Chromosome 1
Transcript - NCBI ID NM_152486.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_689699.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2012-09-13 13:16:37 +02:00 (CEST)
Date last edited N/A


Variants

71 entries on 1 page. Showing entries 1 - 71.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.-1339T>C r.(?) p.(=)
-?/. - c.-1132C>T r.(?) p.(=)
-?/. - c.-922C>T r.(?) p.(=)
?/. - c.58A>G r.(?) p.(Ile20Val)
?/. - c.72+990C>T r.(=) p.(=)
-?/. - c.83G>A r.(?) p.(Arg28Gln)
?/. - c.171C>A r.(?) p.(Asp57Glu)
?/. - c.222G>T r.(?) p.(Glu74Asp)
-/. - c.232C>T r.(?) p.(His78Tyr)
-/. - c.258C>T r.(?) p.(=)
-?/. - c.305+7G>A r.(=) p.(=)
-?/. - c.306-20T>C r.(=) p.(=)
-/. - c.313G>A r.(?) p.(Gly105Ser)
-?/. - c.431-5C>T r.spl? p.?
-?/. - c.508G>A r.(?) p.(Glu170Lys)
-?/. - c.600C>T r.(?) p.(Ser200=)
-?/. - c.600C>T r.(?) p.(Ser200=)
-?/. - c.646C>T r.(?) p.(Leu216Phe)
+?/. 8 c.682_683insT r.(?) p.(Pro228Leufs*227)
+?/. 8 c.682_683insT r.(?) p.(Pro228Leufs*227)
-/. - c.683_706+24del r.spl? p.?
-?/. - c.706_706+48del r.spl? p.?
-?/. - c.706+7A>G r.(=) p.(=)
?/. 9 c.826C>G r.(?) p.(Arg276Gly)
-?/. - c.858C>G r.(?) p.(Ser286=)
?/. - c.860T>C r.(?) p.(Phe287Ser)
?/. - c.910G>A r.(?) p.(Ala304Thr)
-?/. - c.930C>T r.(?) p.(Gly310=)
?/. - c.944C>T r.(?) p.(Pro315Leu)
-?/. - c.948C>T r.(?) p.(Pro316=)
?/. - c.962C>T r.(?) p.(Pro321Leu)
-?/. - c.981C>T r.(?) p.(Thr327=)
-?/. - c.1065-7G>C r.(=) p.(=)
-?/. - c.1104G>A r.(?) p.(Leu368=)
-?/. - c.1104G>A r.(?) p.(Leu368=)
-?/. - c.1155C>T r.(?) p.(Asn385=)
-?/. - c.1155C>T r.(?) p.(Asn385=)
?/. - c.1179del r.(?) p.(Arg394Alafs*7)
-?/. - c.1285C>T r.(?) p.(Arg429Trp)
?/. - c.1368G>A r.(?) p.(Trp456*)
?/. 11 c.1454C>T r.(?) p.(Ser485Leu)
-/. - c.1457C>T r.(?) p.(Pro486Leu)
-?/. - c.1564+9C>T r.(=) p.(=)
-?/. - c.1596G>A r.(?) p.(Glu532=)
-?/. - c.1676G>C r.(?) p.(Gly559Ala)
-?/. - c.1689+7G>C r.(=) p.(=)
-?/. - c.1689+11dup r.(=) p.(=)
?/. - c.1754C>T r.(?) p.(Thr585Ile)
-?/. - c.1800+15A>C r.(=) p.(=)
+?/. 14 c.1888C>T r.(?) p.(Arg630*)
+?/. 14 c.1888C>T r.(?) p.(Arg630*)
+?/. 14 c.1888C>T r.(?) p.(Arg630*)
+?/. 14 c.1888C>T r.(?) p.(Arg630*)
+?/. 14 c.1888C>T r.(?) p.(Arg630*)
?/. - c.1888C>T r.(?) p.(Arg630Ter)
-?/. - c.1894C>T r.(?) p.(Leu632Phe)
-?/. - c.1897G>A r.(?) p.(Gly633Ser)
?/. 14 c.1924G>A r.(?) p.(Val642Ile)
-/. - c.1926G>A r.(?) p.(=)
-?/. - c.1935G>A r.(?) p.(Thr645=)
-?/. - c.1935G>T r.(?) p.(Thr645=)
+?/. 14 c.2150dup r.(=) p.(Leu718Profs*186)
-?/. - c.*930C>T r.(=) p.(=)
-?/. - c.*1373G>A r.(=) p.(=)
-/. - c.*2094G>A r.(=) p.(=)
?/. - c.*2272C>A r.(=) p.(=)
-?/. - c.*17804C>T r.(=) p.(=)
-?/. - c.*18197C>T r.(=) p.(=)
-?/. - c.*18607G>A r.(=) p.(=)
?/. - c.*19224G>C r.(=) p.(=)
-?/. - c.*19340C>T r.(=) p.(=)
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