Transcript #00005115

Transcript name transcript variant 2
Gene name EGF (epidermal growth factor)
Chromosome 4
Transcript - NCBI ID NM_001178130.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001171601.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

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

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/? c.-51C>T r.(=) p.(=)
?/? c.-46G>A r.(=) p.(=)
?/? c.46A>C r.(?) p.(Ser16Arg)
?/? c.47G>C r.(?) p.(Ser16Thr)
?/? c.127+29G>T r.(=) p.(=)
?/? c.127+35C>T r.(=) p.(=)
?/? c.127+42C>T r.(=) p.(=)
?/? c.127+46C>T r.(=) p.(=)
?/? c.128-30A>G r.(=) p.(=)
?/? c.176T>C r.(?) p.(Ile59Thr)
?/? c.192C>A r.(=) p.(=)
?/? c.217G>A r.(?) p.(Ala73Thr)
?/? c.264C>T r.(=) p.(=)
?/? c.327+7T>C r.(=) p.(=)
?/? c.327+51_327+55del r.(=) p.(=)
?/? c.448T>A r.(?) p.(Ser150Thr)
?/? c.451C>T r.(?) p.(His151Tyr)
?/? c.464G>A r.(?) p.(Ser155Asn)
?/? c.465T>G r.(?) p.(Ser155Arg)
?/? c.484A>G r.(?) p.(Asn162Asp)
?/? c.509+40A>C r.(=) p.(=)
?/? c.510-14G>A r.(=) p.(=)
?/? c.552A>G r.(=) p.(=)
?/? c.556G>C r.(?) p.(Asp186His)
?/? c.561C>A r.(=) p.(=)
?/? c.637C>T r.(?) p.(Arg213Trp)
?/? c.638G>A r.(?) p.(Arg213Gln)
?/? c.662G>C r.(?) p.(Arg221Thr)
?/? c.687C>A r.(?) p.(Cys229*)
?/? c.723T>C r.(=) p.(=)
?/? c.730C>T r.(?) p.(Pro244Ser)
?/? c.736C>G r.(?) p.(Gln246Glu)
?/? c.737+11C>T r.(=) p.(=)
?/? c.737+39T>C r.(=) p.(=)
?/? c.737+46T>G r.(=) p.(=)
?/? c.737+49A>G r.(=) p.(=)
?/? c.738-51A>C r.(=) p.(=)
?/? c.738-11T>A r.(=) p.(=)
?/? c.769G>C r.(?) p.(Asp257His)
?/? c.837C>T r.(=) p.(=)
?/? c.866T>G r.(?) p.(Phe289Cys)
?/? c.875T>A r.(?) p.(Leu292His)
?/? c.877G>T r.(?) p.(Gly293Cys)
?/? c.891A>C r.(=) p.(=)
?/? c.924T>C r.(=) p.(=)
?/? c.927C>A r.(?) p.(Asp309Glu)
?/? c.940+10C>T r.(=) p.(=)
?/? c.940+11G>A r.(=) p.(=)
?/? c.940+22G>A r.(=) p.(=)
?/? c.941-35C>T r.(=) p.(=)
?/? c.941-9C>A r.(=) p.(=)
?/? c.978C>T r.(=) p.(=)
?/? c.987G>A r.(=) p.(=)
?/? c.1066+10G>C r.(=) p.(=)
?/? c.1066+38C>T r.(=) p.(=)
?/? c.1066+40C>T r.(=) p.(=)
?/? c.1067-23A>G r.(=) p.(=)
?/? c.1095T>C r.(=) p.(=)
?/? c.1097G>A r.(?) p.(Gly366Asp)
?/? c.1100G>A r.(?) p.(Cys367Tyr)
?/? c.1180C>T r.(?) p.(Arg394*)
?/? c.1181G>A r.(?) p.(Arg394Gln)
?/? c.1189C>T r.(?) p.(Gln397*)
?/? c.1189+11G>A r.(=) p.(=)
?/? c.1190-39G>T r.(=) p.(=)
?/? c.1190-23T>C r.(=) p.(=)
?/? c.1190-10T>C r.(=) p.(=)
?/? c.1208G>A r.(?) p.(Arg403His)
?/? c.1244C>A r.(?) p.(Thr415Lys)
?/? c.1253G>T r.(?) p.(Gly418Val)
?/? c.1258T>C r.(=) p.(=)
?/? c.1292G>A r.(?) p.(Arg431Lys)
?/? c.1308T>C r.(=) p.(=)
?/? c.1312+23C>T r.(=) p.(=)
?/? c.1313-33C>T r.(=) p.(=)
?/? c.1313-10G>T r.(=) p.(=)
?/? c.1313-3T>C r.spl? p.?
?/? c.1354G>A r.(?) p.(Val452Ile)
?/? c.1367C>A r.(?) p.(Pro456Gln)
?/? c.1380A>G r.(=) p.(=)
?/? c.1404C>T r.(=) p.(=)
?/? c.1416T>A r.(?) p.(Asp472Glu)
?/? c.1438+35del r.(=) p.(=)
?/? c.1438+35dup r.(=) p.(=)
?/? c.1438+42A>T r.(=) p.(=)
?/? c.1438+47del r.(=) p.(=)
?/? c.1438+48G>A r.(=) p.(=)
?/? c.1439-47T>C r.(=) p.(=)
?/? c.1439-40C>T r.(=) p.(=)
?/? c.1487T>C r.(?) p.(Met496Thr)
?/? c.1491T>C r.(=) p.(=)
?/? c.1496A>G r.(?) p.(Asp499Gly)
?/? c.1521_1524del r.(?) p.(Gln509Argfs*8)
?/? c.1575+6G>T r.(=) p.(=)
?/? c.1575+32A>G r.(=) p.(=)
?/? c.1575+50A>G r.(=) p.(=)
?/? c.1576-37del r.(=) p.(=)
?/? c.1576-37dup r.(=) p.(=)
?/? c.1576-3T>C r.spl? p.?
?/? c.1595C>T r.(?) p.(Ala532Val)
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