Transcript #00006933 (NM_005228.3, EGFR gene)

Transcript name transcript variant 1
Gene name EGFR (epidermal growth factor receptor)
Chromosome 7
Transcript - NCBI ID NM_005228.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_005219.2
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

74 entries on 1 page. Showing entries 1 - 74.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/. - c.? r.(?) p.(Gly573Arg)
-?/. - c.61G>A r.(?) p.(Ala21Thr)
-?/. - c.241-8C>G r.(=) p.(=)
-?/. - c.339C>T r.(?) p.(Tyr113=)
?/. - c.493C>T r.(?) p.(Arg165Trp)
-/. - c.531G>A r.(?) p.(Ser177=)
?/. - c.731G>A r.(?) p.(Arg244Gln)
-?/. - c.758A>G r.(?) p.(Lys253Arg)
+?/. - c.860T>G r.(?) p.(Phe287Cys)
?/. - c.889C>G r.(?) p.(Arg297Gly)
?/. - c.971G>A r.(?) p.(Arg324His)
?/. - c.1039G>T r.(?) p.(Asp347Tyr)
?/. - c.1145C>T r.(?) p.(Thr382Ile)
?/. - c.1145C>T r.(?) p.(Thr382Ile)
?/. - c.1255G>A r.(?) p.(Ala419Thr)
+/. 11 c.1283G>A r.(?) p.(Gly428Asp)
+/. - c.1283G>A r.(?) p.(Gly428Asp)
?/. - c.1333A>G r.(?) p.(Ile445Val)
-?/. - c.1498+10C>T r.(=) p.(=)
-?/. - c.1499-4G>A r.spl? p.?
-/. - c.1509C>T r.(?) p.(Gly503=)
?/. - c.1532C>A r.(?) p.(Ser511Tyr)
-/. - c.1562G>A r.(?) p.(Arg521Lys)
-/. - c.1562G>A r.(?) p.(Arg521Lys)
-?/. - c.1799T>C r.(?) p.(Met600Thr)
?/. - c.1799T>C r.(?) p.(Met600Thr)
+?/. - c.1881-858G>T r.? p.?
?/. - c.1881-780C>T r.(=) p.(=)
-?/. - c.1881-775C>T r.(=) p.(=)
?/. - c.1881-774G>A r.(=) p.(=)
-/. - c.1887T>A r.(?) p.(Thr629=)
?/. - c.1936A>C r.(?) p.(Ile646Leu)
?/. - c.1996C>T r.(?) p.(Leu666Phe)
?/. - c.2024G>A r.(?) p.(Arg675Gln)
-/. - c.2047C>T r.(?) p.(Leu683=)
-?/. - c.2061+17G>A r.(=) p.(=)
+/. - c.2152C>G r.(?) p.(Leu718Val)
+?/. - c.2153T>A r.(?) p.(Leu718Gln)
-?/. - c.2169C>T r.(?) p.(Phe723=)
-/. - c.2184+19G>A r.(=) p.(=)
?/. - c.2254T>A r.(?) p.(Ser752Thr)
+/. 20 c.[2303G>T;2305G>T] r.(?) p.(Ser768_Val769delinsIleLeu)
?/. - c.2305G>A r.(?) p.(Val769Met)
+/. - c.2311_2312insGTC r.(?) p.(Asn771delinsSerHis)
?/. - c.2327G>A r.(?) p.(Arg776His)
-/. - c.2361G>A r.(?) p.(Gln787=)
-?/. - c.2487G>A r.(?) p.(Glu829=)
+/. - c.2497T>G r.(?) p.(Leu833Val)
-/. - c.2508C>T r.(?) p.(Arg836=)
?/. - c.2543C>T r.(?) p.(Pro848Leu)
?/. - c.2543C>T r.(?) p.(Pro848Leu)
?/. - c.2621G>A r.(?) p.(Gly874Asp)
-?/. - c.2626-19C>T r.(=) p.(=)
+?/. - c.2694G>A r.(?) p.(Trp898*)
-/. - c.2709= r.(=) p.(Thr903=)
-?/. - c.2748C>T r.(?) p.(Asp916=)
-?/. - c.2748C>T r.(?) p.(Asp916=)
?/. - c.2842G>A r.(?) p.(Val948Ile)
./. - c.2873G>A r.(?) p.(Arg958His)
?/. - c.2885G>A r.(?) p.(Arg962His)
?/. - c.2885G>A r.(?) p.(Arg962His)
?/. - c.2996G>A r.(?) p.(Arg999His)
-?/. - c.3015A>G r.(?) p.(Glu1005=)
-?/. - c.3015A>G r.(?) p.(Glu1005=)
-?/. - c.3015A>G r.(?) p.(Glu1005=)
-?/. - c.3114+29_3114+30del r.(=) p.(=)
?/. - c.3214G>C r.(?) p.(Asp1072His)
?/. - c.3250_3252del r.(?) p.(Asp1084del)
-?/. - c.3272-9C>T r.(=) p.(=)
-?/. - c.3453C>T r.(?) p.(Phe1151=)
?/. - c.3454G>C r.(?) p.(Asp1152His)
?/. - c.3551A>G r.(?) p.(Asn1184Ser)
-?/. - c.3551A>G r.(?) p.(Asn1184Ser)
?/. - c.3629C>T r.(?) p.(Ala1210Val)
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