Transcript #00018389 (NM_017654.3, SAMD9 gene)

Transcript name transcript variant 1
Gene name SAMD9 (sterile alpha motif domain containing 9)
Chromosome 7
Transcript - NCBI ID NM_017654.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_060124.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/. - c.15T>A r.(?) p.(Leu5=)
-?/. - c.95A>T r.(?) p.(His32Leu)
-/. - c.223C>T r.(?) p.(Arg75Trp)
-?/. - c.246G>A r.(?) p.(=)
-?/. - c.257C>T r.(?) p.(Ser86Phe)
-?/. - c.346G>A r.(?) p.(Gly116Ser)
?/. - c.382A>G r.(?) p.(Met128Val)
-/. - c.428T>C r.(?) p.(Ile143Thr)
-/. - c.428T>C r.(?) p.(Ile143Thr)
-?/. - c.579G>A r.(?) p.(Pro193=)
-?/. - c.609A>G r.(?) p.(Thr203=)
-?/. - c.662G>A r.(?) p.(Arg221Gln)
?/. - c.730del r.(?) p.(His244Metfs*23)
+?/. - c.773A>C r.(?) p.(Glu258Ala)
-?/. - c.854G>A r.(?) p.(Arg285Gln)
-/. - c.960T>C r.(?) p.(Tyr320=)
-?/. - c.982T>C r.(?) p.(Tyr328His)
+/. - c.1030C>T r.(?) p.(Arg344*)
+/. - c.1030C>T r.(?) p.(Arg344*)
+/. - c.1030C>T r.(?) p.(Arg344*)
-?/. - c.1052A>T r.(?) p.(Asp351Val)
-?/. - c.1053C>T r.(?) p.(Asp351=)
?/. - c.1283T>G r.(?) p.(Leu428*)
?/. - c.1308G>A r.(?) p.(Trp436*)
?/. - c.1308G>A r.(?) p.(Trp436*)
-?/. - c.1346A>G r.(?) p.(Asn449Ser)
-/. - c.1346A>G r.(?) p.(Asn449Ser)
-/. - c.1347T>C r.(?) p.(Asn449=)
-/. - c.1347T>C r.(?) p.(Asn449=)
-/. - c.1360G>A r.(?) p.(Ala454Thr)
-?/. - c.1411G>C r.(?) p.(Glu471Gln)
-/. - c.1436C>T r.(?) p.(Thr479Met)
-/. - c.1436C>T r.(?) p.(Thr479Met)
-?/. - c.1528C>T r.(?) p.(Pro510Ser)
?/. - c.1645G>A r.(?) p.(Val549Met)
-/. - c.1645G>T r.(?) p.(Val549Leu)
?/. - c.1667T>C r.(?) p.(Leu556Pro)
-?/. - c.1684G>A r.(?) p.(Ala562Thr)
-?/. - c.1684G>A r.(?) p.(Ala562Thr)
?/. - c.1762G>T r.(?) p.(Asp588Tyr)
?/. - c.1766T>C r.(?) p.(Leu589Pro)
?/. - c.1800_1801del r.(?) p.(Glu600AspfsTer12)
?/. - c.1800_1801del r.(?) p.(Glu600AspfsTer12)
?/. - c.1880del r.(?) p.(Ser627Phefs*16)
+?/. - c.1880del r.(?) p.(Ser627Phefs*16)
?/. - c.1880del r.(?) p.(Ser627Phefs*16)
?/. - c.1912T>C r.(?) p.(Ser638Pro)
-?/. - c.2002G>A r.(?) p.(Asp668Asn)
?/. - c.2004C>G r.(?) p.(Asp668Glu)
+?/. - c.2051A>G r.(?) p.(Tyr684Cys)
?/. - c.2053C>T r.(?) p.(Arg685Ter)
?/. - c.2073G>A r.(?) p.(Trp691*)
?/. - c.2130A>C r.(?) p.(Lys710Asn)
-?/. - c.2254T>A r.(?) p.(Trp752Arg)
?/. - c.2254T>A r.(?) p.(Trp752Arg)
?/. - c.2429del r.(?) p.(Leu810Argfs*9)
+/. - c.2471G>A r.(?) p.(Arg824Gln)
+?/. - c.2569C>T r.(?) p.(Leu857Phe)
-?/. - c.2642A>G r.(?) p.(Asp881Gly)
?/. - c.2645T>G r.(?) p.(Phe882Cys)
-/. - c.2680A>G r.(?) p.(Lys894Glu)
?/. - c.2686T>C r.(?) p.(Tyr896His)
?/. - c.2686T>C r.(?) p.(Tyr896His)
?/. - c.2809_2819del r.(?) p.(Gln937Ilefs*17)
-?/. - c.2845G>T r.(?) p.(Ala949Ser)
-?/. - c.2845G>T r.(?) p.(Ala949Ser)
+/. - c.2920G>A r.(?) p.(Glu974Lys)
+?/. - c.2938G>A r.(?) p.(Gly980Arg)
?/. - c.3005T>C r.(?) p.(Leu1002Pro)
-?/. - c.3008A>G r.(?) p.(Asn1003Ser)
-?/. - c.3008A>G r.(?) p.(Asn1003Ser)
-?/. - c.3008A>G r.(?) p.(Asn1003Ser)
?/. - c.3134G>T r.(?) p.(Gly1045Val)
?/. - c.3142G>A r.(?) p.(Gly1048Arg)
-?/. - c.3171A>G r.(?) p.(Ala1057=)
-?/. - c.3176A>G r.(?) p.(His1059Arg)
-?/. - c.3192T>G r.(?) p.(Asn1064Lys)
-?/. - c.3199G>C r.(?) p.(Val1067Leu)
-?/. - c.3215T>C r.(?) p.(Leu1072Pro)
?/. - c.3215T>C r.(?) p.(Leu1072Pro)
?/. - c.3307C>G r.(?) p.(Leu1103Val)
-?/. - c.3403A>G r.(?) p.(Ile1135Val)
-?/. - c.3651dup r.(?) p.(Asp1218*)
-?/. - c.3651dup r.(?) p.(Asp1218*)
-?/. - c.3713T>G r.(?) p.(Ile1238Ser)
?/. - c.3728_3731del r.(?) p.(Asn1243Metfs*5)
?/. - c.3743T>G r.(?) p.(Leu1248*)
-?/. - c.3764C>T r.(?) p.(Pro1255Leu)
?/. - c.3805del r.(?) p.(Asp1269IlefsTer10)
-/. - c.3812T>C r.(?) p.(Phe1271Ser)
-/. - c.3825T>C r.(?) p.(Phe1275=)
-?/. - c.3825T>C r.(?) p.(Phe1275=)
+?/. - c.3846C>A r.(?) p.(Asn1282Lys)
-?/. - c.3886G>A r.(?) p.(Val1296Met)
?/. - c.3937T>C r.(?) p.(Ser1313Pro)
-?/. - c.4001G>T r.(?) p.(Arg1334Ile)
-?/. - c.4010T>C r.(?) p.(Val1337Ala)
-?/. - c.4067A>G r.(?) p.(Glu1356Gly)
-?/. - c.4067A>G r.(?) p.(Glu1356Gly)
-?/. - c.4102G>A r.(?) p.(Glu1368Lys)
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