Transcript #00019422 (NM_001127207.1, SMARCAL1 gene)

Transcript name transcript variant 2
Gene name SMARCAL1 (SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a-like 1)
Chromosome 2
Transcript - NCBI ID NM_001127207.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001120679.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+/. 2i_4i c.(?_-1)_(862+1_)del r.? p.?
-/. - c.-368C>T r.(?) p.(=)
-?/. - c.-233T>C r.(?) p.(=)
-/. - c.72A>G r.(?) p.(Arg24=)
?/. - c.117C>T r.(?) p.(Gly39=)
-?/. - c.127G>A r.(?) p.(Ala43Thr)
-/. - c.127G>A r.(?) p.(Ala43Thr)
-?/. - c.136C>T r.(?) p.(Pro46Ser)
?/. - c.191C>T r.(?) p.(Pro64Leu)
-/. - c.341G>A r.(?) p.(Arg114His)
+/. - c.415_416del r.(?) p.(Leu139GlufsTer3)
?/. - c.423T>C r.(=) p.(=)
-?/. - c.448G>T r.(?) p.(Ala150Ser)
-?/. - c.603G>C r.(?) p.(Gly201=)
-?/. - c.604C>A r.(?) p.(Gln202Lys)
-?/. - c.644C>T r.(?) p.(Thr215Met)
+?/. - c.670C>T r.(?) p.(Gln224Ter)
-?/. - c.680G>T r.(?) p.(Gly227Val)
-?/. - c.724G>A r.(?) p.(Val242Ile)
-?/. - c.828G>T r.(?) p.(Thr276=)
?/. - c.836T>C r.(?) p.(Phe279Ser)
?/. - c.836T>C r.(?) p.(Phe279Ser)
-?/. - c.862+128del r.(=) p.(=)
-/. - c.862+183G>A r.(=) p.(=)
+/. - c.863-2A>G r.spl? p.?
?/. - c.889G>A r.(?) p.(Val297Ile)
-/. - c.901C>G r.(?) p.(Pro301Ala)
-/. - c.901C>G r.(?) p.(Pro301Ala)
?/. - c.927C>T r.(?) p.(Ser309=)
-?/. - c.934C>G r.(?) p.(Pro312Ala)
-?/. - c.945C>G r.(?) p.(Ser315Arg)
-/. - c.1096+192C>T r.(=) p.(=)
-/. - c.1129G>C r.(?) p.(Glu377Gln)
-/. - c.1129G>C r.(?) p.(Glu377Gln)
-?/. - c.1129G>C r.(?) p.(Glu377Gln)
-/. - c.1147+34C>A r.(=) p.(=)
?/. - c.1159C>T r.(?) p.(Arg387Cys)
-?/. - c.1196C>T r.(?) p.(Thr399Met)
-?/. - c.1196C>T r.(?) p.(Thr399Met)
-?/. - c.1196C>T r.(?) p.(Thr399Met)
-?/. - c.1197G>A r.(?) p.(Thr399=)
-?/. - c.1212G>A r.(?) p.(Ala404=)
-/. - c.1243A>G r.(?) p.(Ser415Gly)
-/. - c.1243A>G r.(?) p.(Ser415Gly)
+/. - c.1248dup r.(?) p.(Thr417Hisfs*11)
-?/. - c.1251G>A r.(?) p.(Thr417=)
-?/. - c.1271A>T r.(?) p.(Asp424Val)
-?/. - c.1271A>T r.(?) p.(Asp424Val)
-?/. - c.1271A>T r.(?) p.(Asp424Val)
-?/. - c.1301C>T r.(?) p.(Ser434Phe)
?/. - c.1301C>T r.(?) p.(Ser434Phe)
?/. - c.1334A>T r.(?) p.(Asn445Ile)
?/. - c.1342A>G r.(?) p.(Ile448Val)
-?/. - c.1349A>G r.(?) p.(Lys450Arg)
+?/. - c.1385T>C r.(?) p.(Leu462Pro)
-?/. - c.1427G>A r.(?) p.(Arg476Gln)
-?/. - c.1464C>T r.(?) p.(=)
?/. - c.1468C>T r.(?) p.(Arg490Cys)
-?/. - c.1534G>A r.(?) p.(Val512Met)
+?/. 9 c.1615C>G r.[1615c>g;1615_1644del] p.[Leu539Val;Leu539_Ile548del]
?/. - c.1682G>A r.(?) p.(Arg561His)
+/. - c.1687C>T r.(?) p.(Arg563*)
?/. - c.1694C>T r.(?) p.(Ala565Val)
-?/. - c.1696A>C r.(?) p.(Met566Leu)
-?/. - c.1785C>T r.(?) p.(Ile595=)
?/. - c.1786G>A r.(?) p.(Ala596Thr)
-?/. - c.1850G>T r.(?) p.(Arg617Leu)
-?/. - c.1851+3A>G r.spl? p.?
-?/. - c.1851+3A>G r.spl? p.?
?/. - c.1851+5G>A r.spl? p.?
?/. - c.1851+5G>A r.spl? p.?
?/. - c.1851+5G>A r.spl? p.?
-?/. - c.1908G>A r.(?) p.(Leu636=)
-?/. - c.1947C>T r.(?) p.(=)
-?/. - c.1995C>T r.(?) p.(Ala665=)
-/. - c.2070T>C r.(?) p.(Thr690=)
-/. - c.2070T>C r.(?) p.(Thr690=)
+/. 12 c.2070+2dup r.[=,1852_2070del] p.[=,Met618_Thr690del]
+/. - c.2070+2dup r.spl? p.?
+?/. - c.2070+2dup r.spl? p.?
+?/. - c.2070+2dup r.spl? p.?
+?/. 13 c.2114C>T r.(?) p.(Thr705Ile)
+?/. - c.2114C>T r.(?) p.(Thr705Ile)
?/. - c.2114C>T r.(?) p.(Thr705Ile)
-/. - c.2141+17T>C r.(=) p.(=)
-/. - c.2141+55A>C r.(=) p.(=)
-/. - c.2141+56dup r.(=) p.(=)
-?/. - c.2225C>T r.(?) p.(Thr742Met)
-?/. - c.2225C>T r.(?) p.(Thr742Met)
-?/. - c.2226G>A r.(?) p.(Thr742=)
-?/. - c.2248G>A r.(?) p.(Val750Met)
?/. - c.2263A>G r.(?) p.(Ile755Val)
-?/. - c.2427+9C>T r.(=) p.(=)
-/. - c.2428-95G>A r.(=) p.(=)
-?/. - c.2454G>A r.(?) p.(Val818=)
-?/. - c.2528+15G>A r.(=) p.(=)
+/. - c.2542G>T r.(?) p.(Glu848Ter)
-?/. - c.2641A>C r.(?) p.(Lys881Gln)
-?/. - c.2641A>C r.(?) p.(Lys881Gln)
?/. - c.2644A>G r.(?) p.(Ile882Val)
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