Transcript #00007751 (NM_024582.4, FAT4 gene)

Transcript name FAT tumor suppressor homolog 4 (Drosophila)
Gene name FAT4 (FAT tumor suppressor homolog 4 (Drosophila))
Chromosome 4
Transcript - NCBI ID NM_024582.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_078858.4
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

471 entries on 5 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/. - c.? r.(?) p.(Glu4734Gly)
?/. - c.? r.(?) p.(Ala2178Val)
?/. - c.? r.(?) p.(Glu3862Gln)
?/. - c.? r.(?) p.(Arg1804Gly)
?/. - c.65C>G r.(?) p.(Ser22Cys)
?/. - c.104C>T r.(?) p.(Pro35Leu)
-?/. - c.104C>T r.(?) p.(Pro35Leu)
?/. - c.155T>C r.(?) p.(Leu52Pro)
-?/. - c.185G>C r.(?) p.(Gly62Ala)
?/. - c.185G>C r.(?) p.(Gly62Ala)
-?/. - c.185G>C r.(?) p.(Gly62Ala)
?/. - c.211A>G r.(?) p.(Thr71Ala)
-?/. - c.283A>T r.(?) p.(Thr95Ser)
-?/. - c.288C>A r.(?) p.(Ile96=)
-?/. - c.298A>G r.(?) p.(Ser100Gly)
?/. - c.386A>G r.(?) p.(Asn129Ser)
-/. - c.405C>T r.(?) p.(Phe135=)
-/. - c.405C>T r.(?) p.(Phe135=)
?/. - c.418A>G r.(?) p.(Ile140Val)
?/. - c.502G>C r.(?) p.(Gly168Arg)
?/. - c.523C>A r.(?) p.(Arg175Ser)
?/. - c.524G>T r.(?) p.(Arg175Leu)
?/. - c.524G>T r.(?) p.(Arg175Leu)
-?/. - c.524G>T r.(?) p.(Arg175Leu)
-?/. - c.524G>T r.(?) p.(Arg175Leu)
?/. - c.524G>T r.(?) p.(Arg175Leu)
-?/. - c.544G>T r.(?) p.(Ala182Ser)
-?/. - c.546G>A r.(?) p.(Ala182=)
-?/. - c.739C>A r.(?) p.(Pro247Thr)
-/. - c.739C>A r.(?) p.(Pro247Thr)
-/. - c.739C>A r.(?) p.(Pro247Thr)
-/. - c.739C>A r.(?) p.(Pro247Thr)
-?/. - c.739C>A r.(?) p.(Pro247Thr)
?/. - c.739C>A r.(?) p.(Pro247Thr)
-?/. - c.739C>T r.(?) p.(Pro247Ser)
./. - c.739C>T r.(?) p.(Pro247Ser)
?/. - c.778C>A r.(?) p.(Pro260Thr)
?/. - c.821C>T r.(?) p.(Ala274Val)
?/. - c.829G>A r.(?) p.(Ala277Thr)
-?/. - c.829G>A r.(?) p.(Ala277Thr)
-?/. - c.831G>A r.(?) p.(Ala277=)
?/. - c.842C>T r.(?) p.(Thr281Ile)
-?/. - c.900T>A r.(?) p.(Pro300=)
-?/. - c.1101A>G r.(?) p.(Val367=)
-/. - c.1101A>G r.(?) p.(Val367=)
-/. - c.1101A>G r.(?) p.(Val367=)
-/. - c.1128G>A r.(?) p.(Val376=)
-?/. - c.1128G>A r.(?) p.(Val376=)
?/. - c.1244C>G r.(?) p.(Pro415Arg)
?/. - c.1244C>G r.(?) p.(Pro415Arg)
?/. - c.1263G>C r.(?) p.(Lys421Asn)
?/. - c.1295dup r.(?) p.(Ser433PhefsTer10)
-?/. - c.1299C>G r.(?) p.(Ser433=)
-?/. - c.1299C>G r.(?) p.(Ser433=)
-?/. - c.1299C>G r.(?) p.(Ser433=)
-/. - c.1358A>T r.(?) p.(Gln453Leu)
-/. - c.1358A>T r.(?) p.(Gln453Leu)
?/. - c.1381C>G r.(?) p.(Leu461Val)
-?/. - c.1432C>G r.(?) p.(Gln478Glu)
-?/. - c.1449C>T r.(?) p.(Asn483=)
?/. - c.1495G>A r.(?) p.(Ala499Thr)
?/. - c.1526A>G r.(?) p.(Asn509Ser)
-?/. - c.1608C>T r.(?) p.(Ser536=)
?/. - c.1660G>A r.(?) p.(Ala554Thr)
?/. - c.1807T>A r.(?) p.(Leu603Met)
?/. - c.2039T>C r.(?) p.(Leu680Pro)
?/. - c.2057G>A r.(?) p.(Ser686Asn)
-?/. - c.2061T>C r.(?) p.(Pro687=)
-?/. - c.2121C>T r.(?) p.(Tyr707=)
?/. - c.2165G>A r.(?) p.(Gly722Asp)
-?/. - c.2220T>C r.(?) p.(Ala740=)
-?/. - c.2273C>T r.(?) p.(Ala758Val)
?/. - c.2283G>T r.(?) p.(Leu761Phe)
?/. - c.2283G>T r.(?) p.(Leu761Phe)
-?/. - c.2289A>G r.(?) p.(Ile763Met)
-?/. - c.2316A>G r.(?) p.(Gln772=)
-?/. - c.2322C>T r.(?) p.(Pro774=)
-/. - c.2420C>T r.(?) p.(Ala807Val)
-/. - c.2420C>T r.(?) p.(Ala807Val)
-?/. - c.2421G>A r.(?) p.(Ala807=)
?/. - c.2479A>T r.(?) p.(Ser827Cys)
?/. - c.2480G>T r.(?) p.(Ser827Ile)
+?/. - c.2575C>T r.(?) p.(Gln859Ter)
?/. - c.2641A>G r.(?) p.(Ile881Val)
?/. - c.2642T>C r.(?) p.(Ile881Thr)
?/. - c.2689A>G r.(?) p.(Ile897Val)
-?/. - c.2708_2710del r.(?) p.(Val903del)
?/. - c.2708_2710del r.(?) p.(Val903del)
?/. - c.2824A>G r.(?) p.(Ile942Val)
./. - c.2842A>G r.(?) p.(Thr948Ala)
?/. - c.2858G>T r.(?) p.(Gly953Val)
?/. - c.2858G>T r.(?) p.(Gly953Val)
-?/. - c.2898C>A r.(?) p.(Ile966=)
-?/. - c.2919C>T r.(?) p.(Val973=)
-?/. - c.2919C>T r.(?) p.(Val973=)
-/. - c.2944T>C r.(?) p.(Leu982=)
-/. - c.2944T>C r.(?) p.(Leu982=)
?/. - c.2948C>G r.(?) p.(Thr983Arg)
-?/. - c.3012C>A r.(?) p.(Thr1004=)
-/. - c.3096A>G r.(?) p.(Ala1032=)
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