Transcript #00010029 (NM_022489.3, INF2 gene)

Transcript name transcript variant 1
Gene name INF2 (inverted formin, FH2 and WH2 domain containing)
Chromosome 14
Transcript - NCBI ID NM_022489.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_071934.3
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

204 entries on 3 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-/. - c.-85G>A r.(?) p.(=)
-/. - c.-10G>A r.(?) p.(=)
-?/. - c.-10+16C>A r.(=) p.(=)
+?/. - c.(?_-1)_(*1_?)dup r.= p.=
-?/. - c.18C>T r.(?) p.(=)
?/. - c.27dup r.(?) p.(Lys10GlnfsTer136)
-/. - c.42G>A r.(?) p.(Leu14=)
-/. - c.42G>A r.(?) p.(Leu14=)
-?/. - c.67T>A r.(?) p.(Ser23Thr)
-?/. - c.67T>A r.(?) p.(Ser23Thr)
-/. - c.105C>T r.(?) p.(Pro35=)
-/. - c.105C>T r.(?) p.(Pro35=)
-/. - c.105C>T r.(?) p.(Pro35=)
+/. - c.158T>G r.(?) p.(Leu53Arg)
?/. - c.204C>G r.(?) p.(Phe68Leu)
+/. - c.217G>A r.(?) p.(Gly73Ser)
+/. - c.217G>C r.(?) p.(Gly73Arg)
+/. - c.217G>T r.(?) p.(Gly73Cys)
+?/. - c.218G>T r.(?) p.(Gly73Val)
-?/. - c.264C>T r.(?) p.(=)
+/. - c.310T>C r.(?) p.(Cys104Arg)
+/. - c.326T>G r.(?) p.(Met109Arg)
+/. - c.341G>A r.(?) p.(Gly114Asp)
-/. - c.391+6C>T r.(=) p.(=)
-/. - c.391+6C>T r.(=) p.(=)
-/. - c.391+6C>T r.(=) p.(=)
-/. - c.391+17G>A r.(=) p.(=)
-/. - c.391+18A>T r.(=) p.(=)
-?/. - c.408C>T r.(?) p.(=)
-?/. - c.474C>T r.(?) p.(His158=)
-?/. - c.474C>T r.(?) p.(His158=)
+?/. - c.485T>C r.(?) p.(Leu162Pro)
?/. - c.490G>A r.(?) p.(Ala164Thr)
+?/. 3 c.490G>C r.(?) p.(Ala164Pro)
-?/. - c.507+7G>A r.(=) p.(=)
+?/. - c.529C>T r.(?) p.(Arg177Cys)
?/. - c.544A>G r.(?) p.Met182Val
+/. - c.550G>A r.(?) p.(Glu184Lys)
+?/. - c.578A>G r.(?) p.(Tyr193Cys)
?/. - c.586A>T r.(?) p.(Thr196Ser)
-?/. - c.597C>T r.(?) p.(Ser199=)
?/. - c.607G>A r.(?) p.(Ala203Thr)
-/. - c.609C>T r.(?) p.(Ala203=)
-/. - c.610G>A r.(?) p.(Val204Ile)
-?/. - c.636C>T r.(?) p.(Arg212=)
+/. - c.653G>A r.(?) p.(Arg218Gln)
+?/. 4 c.658G>A r.(?) p.(Glu220Lys)
-/. - c.668-46C>T r.(=) p.(=)
-?/. - c.668-12G>A r.(=) p.(=)
+?/. - c.671T>G r.(?) p.(Leu224Arg)
-?/. - c.782G>A r.(?) p.(Arg261Gln)
-?/. - c.798C>G r.(?) p.(Val266=)
-?/. - c.799G>A r.(?) p.(Asp267Asn)
-/. - c.843+16C>T r.(=) p.(=)
-/. - c.843+16C>T r.(=) p.(=)
-?/. - c.844-6G>A r.(=) p.(=)
-?/. - c.858G>A r.(?) p.(Pro286=)
-/. - c.879G>A r.(?) p.(Ser293=)
-/. - c.879G>A r.(?) p.(Ser293=)
-?/. - c.885G>A r.(?) p.(Leu295=)
-?/. - c.885G>A r.(?) p.(Leu295=)
?/. - c.1003G>C r.(?) p.(Glu335Gln)
-/. - c.1049C>T r.(?) p.(Pro350Leu)
-?/. - c.1050G>C r.(?) p.(Pro350=)
-?/. - c.1144A>G r.(?) p.(Ser382Gly)
-?/. - c.1144A>G r.(?) p.(Ser382Gly)
-?/. - c.1182C>T r.(?) p.(=)
?/. - c.1198G>A r.(?) p.(Ala400Thr)
?/. - c.1221A>T r.(?) p.(Lys407Asn)
-/. - c.1227G>T r.(?) p.(Ser409=)
-/. - c.1227G>T r.(?) p.(Ser409=)
-/. - c.1263A>C r.(?) p.(Pro421=)
-/. - c.1269A>C r.(?) p.(Pro423=)
-/. - c.1274_1285del r.(?) p.(Pro425_Pro428del)
-/. - c.1275A>C r.(?) p.(Pro425=)
-/. - c.1280_1285del r.(?) p.(Pro427_Pro428del)
-/. - c.1280_1285del r.(?) p.(Pro427_Pro428del)
-/. - c.1281A>C r.(?) p.(Pro427=)
-/. - c.1281_1286del r.(?) p.(Pro428_Leu429del)
-/. - c.1286_1289del r.(?) p.(Leu429Profs*128)
?/. - c.1309C>T r.(?) p.(Pro437Ser)
?/. - c.1360C>T r.(?) p.(Leu454Phe)
+?/. - c.1372C>T r.(?) p.(Pro458Ser)
?/. - c.1438C>G r.(?) p.(Leu480Val)
-?/. - c.1448C>T r.(?) p.(Ser483Phe)
-/. - c.1451G>A r.(?) p.(Cys484Tyr)
-?/. - c.1451G>A r.(?) p.(Cys484Tyr)
-?/. - c.1451G>A r.(?) p.(Cys484Tyr)
-?/. - c.1452T>C r.(?) p.(Cys484=)
-?/. - c.1458C>T r.(?) p.(Phe486=)
-?/. - c.1500G>C r.(?) p.(Pro500=)
-/. - c.1547C>T r.(?) p.(Pro516Leu)
-/. - c.1582C>T r.(?) p.(Pro528Ser)
-/. - c.1582C>T r.(?) p.(Pro528Ser)
-/. - c.1587C>T r.(?) p.(=)
-?/. - c.1593G>A r.(?) p.(Ala531=)
-?/. - c.1614C>T r.(?) p.(Ile538=)
-?/. - c.1732C>T r.(?) p.(Arg578Cys)
-/. - c.1735+73G>A r.(=) p.(=)
-/. - c.1736-6C>T r.(=) p.(=)
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