Transcript #00007749 (NM_001447.2, FAT2 gene)

Transcript name FAT tumor suppressor homolog 2 (Drosophila)
Gene name FAT2 (FAT tumor suppressor homolog 2 (Drosophila))
Chromosome 5
Transcript - NCBI ID NM_001447.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_001438.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.165C>T r.(?) p.(Phe55=)
-?/. - c.188C>T r.(?) p.(Ala63Val)
?/. - c.397C>T r.(?) p.(Arg133Cys)
-?/. - c.602G>C r.(?) p.(Gly201Ala)
?/. - c.719C>T r.(?) p.(Ala240Val)
-/. - c.789A>G r.(?) p.(Pro263=)
-?/. - c.827T>C r.(?) p.(Leu276Pro)
-/. - c.829G>C r.(?) p.(Val277Leu)
-?/. - c.981T>A r.(?) p.(His327Gln)
-?/. - c.1007G>A r.(?) p.(Arg336Lys)
-?/. - c.1086C>G r.(?) p.(Phe362Leu)
?/. - c.1086C>G r.(?) p.(Phe362Leu)
?/. - c.1103G>A r.(?) p.(Arg368Lys)
-?/. - c.1138C>T r.(?) p.(Arg380Cys)
?/. - c.1150G>A r.(?) p.(Val384Met)
-/. - c.1273G>A r.(?) p.(Asp425Asn)
-?/. - c.1453C>T r.(?) p.(Arg485Trp)
?/. - c.1454G>A r.(?) p.(Arg485Gln)
-?/. - c.1677C>T r.(?) p.(Asp559=)
-?/. - c.1750A>T r.(?) p.(Met584Leu)
-?/. - c.1880A>G r.(?) p.(Asn627Ser)
-?/. - c.1903A>C r.(?) p.(Ser635Arg)
?/. - c.2165T>C r.(?) p.(Ile722Thr)
?/. - c.2444A>G r.(?) p.(Asp815Gly)
-?/. - c.2448C>T r.(?) p.(Asn816=)
-/. - c.2464C>T r.(?) p.(Pro822Ser)
?/. - c.2485A>G r.(?) p.(Ile829Val)
?/. - c.2647C>A r.(?) p.(Arg883Ser)
?/. - c.2650G>A r.(?) p.(Glu884Lys)
?/. - c.2650G>A r.(?) p.(Glu884Lys)
?/. - c.2884T>C r.(?) p.(Tyr962His)
-?/. - c.2918G>T r.(?) p.(Arg973Leu)
?/. - c.2926dup r.(?) p.(Leu976ProfsTer15)
-?/. - c.2940G>C r.(?) p.(Ala980=)
-?/. - c.2991G>A r.(?) p.(Leu997=)
?/. - c.3028C>T r.(?) p.(Arg1010Cys)
-?/. - c.3028C>T r.(?) p.(Arg1010Cys)
?/. - c.3028C>T r.(?) p.(Arg1010Cys)
?/. - c.3135C>A r.(?) p.(Ser1045Arg)
-?/. - c.3175G>A r.(?) p.(Asp1059Asn)
?/. - c.3386A>G r.(?) p.(Asp1129Gly)
-?/. - c.3399C>A r.(?) p.(Asn1133Lys)
-?/. - c.3399C>A r.(?) p.(Asn1133Lys)
?/. - c.3475C>A r.(?) p.(Leu1159Met)
-?/. - c.3555T>C r.(?) p.(Phe1185=)
-?/. - c.4043C>G r.(?) p.(Ala1348Gly)
-?/. - c.4089T>C r.(?) p.(Pro1363=)
-?/. - c.4116C>T r.(?) p.(Ser1372=)
-?/. - c.4207G>A r.(?) p.(Val1403Ile)
-?/. - c.4239G>A r.(?) p.(Arg1413=)
-?/. - c.4239G>C r.(?) p.(Arg1413Ser)
+?/. - c.4370T>C r.(?) p.(Val1457Ala)
-?/. - c.4405C>A r.(?) p.(Arg1469=)
-?/. - c.4563C>T r.(?) p.(His1521=)
?/. - c.4640A>T r.(?) p.(Asp1547Val)
?/. - c.4732C>T r.(?) p.(Arg1578Ter)
-?/. - c.4868A>G r.(?) p.(His1623Arg)
-?/. - c.4983A>G r.(?) p.(Ser1661=)
-?/. - c.5019C>T r.(?) p.(Ile1673=)
-?/. - c.5079G>A r.(?) p.(Glu1693=)
-?/. - c.5230G>C r.(?) p.(Val1744Leu)
-?/. - c.5280G>A r.(?) p.(Lys1760=)
?/. - c.5420C>T r.(?) p.(Pro1807Leu)
-?/. - c.5424G>A r.(?) p.(Glu1808=)
-?/. - c.5477C>T r.(?) p.(Ser1826Leu)
-/. - c.5545G>A r.(?) p.(Val1849Ile)
-?/. - c.5642T>C r.(?) p.(Ile1881Thr)
-?/. - c.5670G>C r.(?) p.(Glu1890Asp)
-?/. - c.5726C>T r.(?) p.(Thr1909Ile)
?/. - c.5837G>A r.(?) p.(Gly1946Asp)
-?/. - c.5916C>T r.(?) p.(Val1972=)
?/. - c.6040A>G r.(?) p.(Met2014Val)
?/. - c.6149G>A r.(?) p.(Arg2050Gln)
+/. - c.6150_6151del r.(?) p.(Val2051Glyfs*10)
-?/. - c.6449C>T r.(?) p.(Thr2150Met)
?/. - c.6449C>T r.(?) p.(Thr2150Met)
?/. - c.6461A>C r.(?) p.(Gln2154Pro)
-?/. - c.6974A>G r.(?) p.(Asn2325Ser)
-?/. - c.6974A>G r.(?) p.(Asn2325Ser)
-?/. - c.7308T>C r.(?) p.(Ile2436=)
+?/. - c.7394_7395del r.(?) p.(Val2465Alafs*22)
-?/. - c.7413T>C r.(?) p.(Thr2471=)
?/. - c.7502T>C r.(?) p.(Ile2501Thr)
-?/. - c.7536C>G r.(?) p.(Pro2512=)
?/. - c.7646C>G r.(?) p.(Thr2549Arg)
-?/. - c.7701C>T r.(?) p.(Ala2567=)
-?/. - c.7780A>G r.(?) p.(Ile2594Val)
-?/. - c.7989C>G r.(?) p.(Ala2663=)
?/. - c.7995T>G r.(?) p.(Asp2665Glu)
-?/. - c.8111T>G r.(?) p.(Leu2704Arg)
-?/. - c.8328T>G r.(?) p.(Asp2776Glu)
-?/. - c.8621A>G r.(?) p.(His2874Arg)
?/. - c.8860C>A r.(?) p.(Gln2954Lys)
-?/. - c.9010G>A r.(?) p.(Val3004Ile)
-?/. - c.9063T>C r.(?) p.(His3021=)
-?/. - c.9193+7T>A r.(=) p.(=)
?/. - c.9277C>T r.(?) p.(Arg3093Ter)
?/. - c.9341T>C r.(?) p.(Phe3114Ser)
?/. - c.9386A>G r.(?) p.(Lys3129Arg)
?/. - c.9497C>T r.(?) p.(Thr3166Met)
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