Transcript #00018390 (NM_152703.2, SAMD9L gene)

Transcript name sterile alpha motif domain containing 9-like
Gene name SAMD9L (sterile alpha motif domain containing 9-like)
Chromosome 7
Transcript - NCBI ID NM_152703.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_689916.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

89 entries on 1 page. Showing entries 1 - 89.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/. - c.10C>T r.(?) p.(Gln4*)
?/. - c.99C>A r.(?) p.(Tyr33*)
?/. - c.154G>C r.(?) p.(Glu52Gln)
-?/. - c.184T>C r.(?) p.(Trp62Arg)
-/. - c.303G>A r.(?) p.(Gln101=)
-?/. - c.384T>C r.(?) p.(Asp128=)
-?/. - c.405T>C r.(?) p.(Ile135=)
-?/. - c.421G>A r.(?) p.(Val141Met)
?/. - c.505G>C r.(?) p.(Asp169His)
?/. - c.668G>A r.(?) p.(Arg223Gln)
-/. - c.796G>A r.(?) p.(Val266Ile)
?/. - c.853C>T r.(?) p.(Arg285Trp)
-/. - c.866T>C r.(?) p.(Phe289Ser)
-?/. - c.866T>C r.(?) p.(Phe289Ser)
?/. - c.1022T>C r.(?) p.(Leu341Pro)
?/. - c.1075C>T r.(?) p.(Arg359Trp)
-?/. - c.1179T>C r.(?) p.(=)
-?/. - c.1214A>C r.(?) p.(Asn405Thr)
-/. - c.1217G>A r.(?) p.(Arg406Gln)
?/. - c.1252A>G r.(?) p.(Ile418Val)
-?/. - c.1503A>G r.(?) p.(Arg501=)
-?/. - c.1503A>G r.(?) p.(Arg501=)
-?/. - c.1503A>G r.(?) p.(Arg501=)
?/. - c.1549T>C r.(?) p.(Trp517Arg)
-?/. - c.1549T>C r.(?) p.(Trp517Arg)
-?/. - c.1565C>T r.(?) p.(Ala522Val)
-?/. - c.1660G>A r.(?) p.(Glu554Lys)
-?/. - c.1696G>A r.(?) p.(Ala566Thr)
-?/. - c.1696G>A r.(?) p.(Ala566Thr)
?/. - c.1877C>T r.(?) p.(Ser626Leu)
-?/. - c.1908C>T r.(?) p.(Pro636=)
-?/. - c.1908C>T r.(?) p.(Pro636=)
-?/. - c.1909G>A r.(?) p.(Ala637Thr)
-?/. - c.1913G>A r.(?) p.(Arg638His)
-?/. - c.1913G>A r.(?) p.(Arg638His)
?/. - c.1916G>A r.(?) p.(Gly639Glu)
-?/. - c.1918T>G r.(?) p.(Ser640Ala)
-?/. - c.1918T>G r.(?) p.(Ser640Ala)
-?/. - c.1954G>A r.(?) p.(Val652Ile)
-?/. - c.1995A>C r.(?) p.(Thr665=)
?/. - c.2065C>T r.(?) p.(Arg689*)
?/. - c.2069G>A r.(?) p.(Gly690Asp)
-?/. - c.2069G>A r.(?) p.(Gly690Asp)
?/. - c.2158G>A r.(?) p.(Asp720Asn)
-?/. - c.2250G>C r.(?) p.(Leu750=)
?/. - c.2419G>A r.(?) p.(Glu807Lys)
?/. - c.2488G>T r.(?) p.(Glu830Ter)
?/. - c.2488G>T r.(?) p.(Glu830Ter)
-/. - c.2604T>C r.(?) p.(Ala868=)
+?/. - c.2640C>A r.(?) p.(His880Gln)
?/. - c.2660A>G r.(?) p.(Tyr887Cys)
?/. - c.2731G>A r.(?) p.(Gly911Arg)
?/. - c.2849_2852dup r.(?) p.(Ser952Hisfs*2)
?/. - c.2849_2852dup r.(?) p.(Ser952Hisfs*2)
-?/. - c.2850C>T r.(?) p.(Tyr950=)
+/. - c.2956C>T r.(?) p.(Arg986Cys)
+?/. - c.2957G>A r.(?) p.(Arg986His)
?/. - c.2957G>A r.(?) p.(Arg986His)
+?/. - c.2957G>A r.(?) p.(Arg986His)
-?/. - c.3027T>C r.(?) p.(Cys1009=)
-/. - c.3027T>C r.(?) p.(Cys1009=)
-/. - c.3028C>G r.(?) p.(Gln1010Glu)
-?/. - c.3102T>C r.(?) p.(Asp1034=)
?/. - c.3127C>T r.(?) p.(Gln1043*)
?/. - c.3130C>T r.(?) p.(Arg1044Cys)
-?/. - c.3285A>G r.(?) p.(Lys1095=)
-?/. - c.3285A>G r.(?) p.(Lys1095=)
?/. - c.3319C>T r.(?) p.(Arg1107Cys)
?/. - c.3377T>C r.(?) p.(Val1126Ala)
-/. - c.3410G>C r.(?) p.(Gly1137Ala)
-?/. - c.3410G>C r.(?) p.(Gly1137Ala)
?/. - c.3563G>C r.(?) p.(Arg1188Pro)
?/. - c.3802T>C r.(?) p.(Phe1268Leu)
-?/. - c.3855A>G r.(?) p.(Lys1285=)
-?/. - c.4082T>C r.(?) p.(Val1361Ala)
-?/. - c.4082T>C r.(?) p.(Val1361Ala)
?/. - c.4140dup r.(?) p.(Gln1381ThrfsTer77)
?/. - c.4140dup r.(?) p.(Gln1381ThrfsTer77)
?/. - c.4140dup r.(?) p.(Gln1381ThrfsTer77)
?/. - c.4140dup r.(?) p.(Gln1381ThrfsTer77)
-?/. - c.4170G>A r.(?) p.(Leu1390=)
-?/. - c.4232G>A r.(?) p.(Arg1411Gln)
-?/. - c.4259G>A r.(?) p.(Ser1420Asn)
-?/. - c.4358C>T r.(?) p.(Ser1453Leu)
-?/. - c.4393C>T r.(?) p.(Arg1465Cys)
-?/. - c.4540A>G r.(?) p.(Lys1514Glu)
-/. - c.4547A>C r.(?) p.(Asn1516Thr)
-?/. - c.4571G>A r.(?) p.(Arg1524His)
-?/. - c.4571G>A r.(?) p.(Arg1524His)
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