Transcript #00008339

Transcript name insulin receptor substrate 4
Gene name IRS4 (insulin receptor substrate 4)
Chromosome X
Transcript - NCBI ID NM_003604.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_003595.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

89 entries on 1 page. Showing entries 1 - 89.
Legend  

Affects function     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/? c.60G>A r.(=) p.(=)
?/? c.63G>A r.(=) p.(=)
?/? c.69G>A r.(=) p.(=)
?/? c.86T>C r.(?) p.(Val29Ala)
?/? c.93C>G r.(=) p.(=)
?/? c.100C>T r.(?) p.(Leu34Phe)
?/? c.111G>C r.(=) p.(=)
?/? c.125C>T r.(?) p.(Ala42Val)
?/? c.138C>T r.(=) p.(=)
?/? c.174G>A r.(=) p.(=)
?/? c.178A>G r.(?) p.(Thr60Ala)
?/? c.396dup r.(?) p.(Ala133Argfs*100)
?/? c.396_397insCCC r.(?) p.(Ala132_Ala133insPro)
?/? c.423C>T r.(=) p.(=)
?/? c.454C>T r.(?) p.(Gln152*)
?/? c.475C>A r.(=) p.(=)
?/? c.582C>A r.(=) p.(=)
?/? c.810C>T r.(=) p.(=)
?/? c.840G>A r.(=) p.(=)
?/? c.920T>C r.(?) p.(Leu307Pro)
?/? c.969G>A r.(=) p.(=)
?/? c.1039A>T r.(?) p.(Ile347Phe)
?/? c.1080C>T r.(=) p.(=)
?/? c.1104G>C r.(=) p.(=)
?/? c.1198G>A r.(?) p.(Val400Ile)
?/? c.1232G>A r.(?) p.(Arg411Gln)
?/? c.1233A>T r.(=) p.(=)
?/? c.1250C>T r.(?) p.(Pro417Leu)
?/? c.1264T>A r.(?) p.(Ser422Thr)
?/? c.1298T>C r.(?) p.(Phe433Ser)
?/? c.1305C>T r.(=) p.(=)
?/? c.1315A>T r.(?) p.(Ser439Cys)
?/? c.1330C>T r.(?) p.(Arg444Trp)
?/? c.1385G>A r.(?) p.(Gly462Asp)
?/? c.1463T>A r.(?) p.(Met488Lys)
?/? c.1473C>T r.(=) p.(=)
?/? c.1492G>A r.(?) p.(Gly498Ser)
?/? c.1524T>A r.(?) p.(Asn508Lys)
?/? c.1533C>T r.(=) p.(=)
?/? c.1646G>C r.(?) p.(Gly549Ala)
?/? c.1682G>C r.(?) p.(Gly561Ala)
?/? c.1735G>A r.(?) p.(Gly579Ser)
?/? c.1766G>T r.(?) p.(Gly589Val)
?/? c.1767G>A r.(=) p.(=)
?/? c.1772_1773insG r.(?) p.(Lys592Glnfs*12)
?/? c.1800C>A r.(=) p.(=)
?/? c.1817G>T r.(?) p.(Arg606Leu)
?/? c.1874A>G r.(?) p.(Gln625Arg)
?/? c.1907C>T r.(?) p.(Pro636Leu)
?/? c.1930G>A r.(?) p.(Gly644Ser)
?/? c.1985G>A r.(?) p.(Gly662Glu)
?/? c.2236A>G r.(?) p.(Met746Val)
?/? c.2348C>G r.(?) p.(Ala783Gly)
?/? c.2391G>A r.(=) p.(=)
?/? c.2472C>G r.(?) p.(Asp824Glu)
?/? c.2493G>A r.(?) p.(Met831Ile)
?/? c.2504A>G r.(?) p.(Lys835Arg)
?/? c.2635C>G r.(?) p.(His879Asp)
?/? c.2697T>C r.(=) p.(=)
?/? c.2698A>G r.(?) p.(Lys900Glu)
?/? c.2733G>A r.(=) p.(=)
?/? c.2760C>G r.(?) p.(Asp920Glu)
?/? c.2864C>G r.(?) p.(Ala955Gly)
?/? c.3002C>G r.(?) p.(Pro1001Arg)
?/? c.3019A>G r.(?) p.(Ser1007Gly)
?/? c.3025G>T r.(?) p.(Ala1009Ser)
?/? c.3031G>A r.(?) p.(Glu1011Lys)
?/? c.3034G>A r.(?) p.(Glu1012Lys)
?/? c.3085A>G r.(?) p.(Met1029Val)
?/? c.3105C>T r.(=) p.(=)
?/? c.3195T>C r.(=) p.(=)
?/? c.3215C>T r.(?) p.(Ala1072Val)
?/? c.3280G>A r.(?) p.(Ala1094Thr)
?/? c.3300C>G r.(=) p.(=)
?/? c.3383T>C r.(?) p.(Leu1128Ser)
?/? c.3409G>T r.(?) p.(Ala1137Ser)
?/? c.3426A>G r.(=) p.(=)
?/? c.3472G>A r.(?) p.(Ala1158Thr)
?/? c.3479C>A r.(?) p.(Ala1160Asp)
?/? c.3536A>G r.(?) p.(Gln1179Arg)
?/? c.3552C>T r.(=) p.(=)
?/? c.3585C>T r.(=) p.(=)
?/? c.3659G>T r.(?) p.(Arg1220Leu)
?/? c.3663G>A r.(=) p.(=)
?/? c.3688G>T r.(?) p.(Asp1230Tyr)
?/? c.3769C>A r.(=) p.(=)
?/? c.3773A>C r.(?) p.(*1258Serext*2)
?/? c.*4del r.(=) p.(=)
?/? c.*30G>T r.(=) p.(=)
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