Transcript #00025538 (NM_000503.4, EYA1 gene)

Transcript name transcript variant 3
Gene name EYA1 (eyes absent homolog 1 (Drosophila))
Chromosome 8
Transcript - NCBI ID NM_000503.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_000494.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2020-07-23 09:23:30 +02:00 (CEST)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+/. _1_18_ c.(?_-640)_(*1907_?)del r.827_966del p.Tyr277SerfsTer8
-?/. - c.-5+4A>C r.spl? p.?
+/. _1_18_ c.-640_*1907{0} r.0? p.0?
?/. - c.35G>A r.(?) p.(Arg12His)
-/. - c.58C>G r.(?) p.(Pro20Ala)
?/? - c.65G>A r.(?) p.(Gly22Asp)
?/? - c.107C>T r.(?) p.(Pro36Leu)
-?/. 3 c.107C>T r.(?) p.(Thr36Ile)
?/. - c.124+1G>A r.spl? p.?
-?/. - c.147C>T r.(?) p.(Ser49=)
?/. - c.158C>T r.(?) p.(Ala53Val)
+/+ - c.164C>T r.(?) p.(Thr55Met)
?/. - c.164C>T r.(?) p.(Thr55Met)
?/. - c.164C>T r.(?) p.(Thr55Met)
?/. - c.197G>T r.(?) p.(Gly66Val)
-?/. - c.197G>T r.(?) p.(Gly66Val)
+?/. - c.229C>T r.(?) p.(Arg77*)
+/. - c.256C>T r.(?) p.(Gln86Ter)
+/+ - c.283C>T r.(?) p.(Pro95Ser)
?/? - c.299C>A r.(?) p.(Thr100Asn)
+?/. - c.319G>A r.(?) p.(Ala107Thr)
+/+ - c.321del r.(?) p.(Tyr108Ilefs*11)
-?/. - c.321T>C r.(?) p.(Ala107=)
+/. - c.337C>T r.(?) p.(Gln113Ter)
+/+ - c.348del r.(?) p.(Tyr117Ilefs*2)
?/. - c.361G>A r.(?) p.(Ala121Thr)
+/. - c.381C>A r.(?) p.(Tyr127Ter)
+/. - c.385C>T r.(?) p.(Gln129*)
+/+ - c.398_405del r.(?) p.(Pro133HisfsTer14)
+/+ - c.402C>A r.(?) p.(Tyr134*)
+/+ - c.403G>A r.(?) p.(Gly135Ser)
+/. - c.403G>A r.(?) p.(Gly135Ser)
+/+ - c.418G>A r.(?) p.(Gly140Ser)
+/. - c.425T>A r.(?) p.(Leu142*)
+/+ - c.428G>A r.(?) p.(Trp143*)
?/. - c.434G>A r.(?) p.(Gly145Asp)
+/+ - c.450_451del r.(?) p.(Gly151IlefsTer36)
+/+ - c.466C>T r.(?) p.(Gln156*)
+/. - c.466C>T r.(?) p.(Gln156*)
+/. - c.478C>T r.(?) p.(Gln160*)
+/+ - c.489dup r.(?) p.(Leu164SerfsTer24)
+/+ - c.529C>T r.(?) p.(Gln177*)
+/. - c.532del r.(?) p.(Ala178HisfsTer63)
+/+ - c.553C>T r.(?) p.(Gln185*)
?/. - c.556+8T>A r.(=) p.(=)
-/. - c.556+18G>T r.(=) p.(=)
+/. 7i c.557-2A>G r.spl p.?
+/+ - c.557-2A>G r.spl? p.?
+/. - c.557-2A>G r.spl? p.?
?/. - c.559A>G r.(?) p.(Ser187Gly)
+/+ - c.588T>A r.(?) p.(Asp196Glu)
+/. 8 c.588_589del r.(?) p.(Thr197Argfs*3)
+/+ - c.592G>T r.(?) p.(Asp198Tyr)
+/+ - c.599dup r.(?) p.(Asn200LysfsTer10)
+/+ - c.602C>G r.(?) p.(Ser201*)
+/+ - c.605T>C r.(?) p.(Val202Ala)
+/. - c.619_622del r.(?) p.(Gly207LeufsTer33)
-?/. - c.630T>C r.(?) p.(Ser210=)
+/+ - c.632C>G r.(?) p.(Ser211*)
+/+ - c.634C>T r.(?) p.(Gln212*)
+/+ - c.638A>T r.(?) p.(Gln213Leu)
+/+ - c.639G>C r.(?) p.(Gln213His)
+/+ - c.639+1G>A r.spl? p.?
+/. 7i c.639+1G>A r.spl p.?
+/+ - c.639+1G>C r.spl? p.?
+/+ - c.639+2del r.spl? p.?
+/+ - c.640-15G>A r.spl? p.(=)
+/. - c.640-2A>C r.spl? p.?
+/+ - c.647C>T r.(?) p.(Ser216Phe)
-?/. - c.648G>A r.(?) p.(Pro216=)
+/+ - c.654T>A r.(?) p.(Tyr218Ter)
+/. 9 c.654T>A r.(?) p.(Tyr218*)
+?/. - c.667C>T r.(?) p.(Gln223*)
+/+ - c.671G>T r.(?) p.(Gly224Val)
?/. - c.671G>T r.(?) p.(Gly224Val)
+/+ - c.678C>G r.(?) p.(Tyr226*)
?/. - c.701C>T r.(?) p.(Pro234Leu)
?/. - c.701C>T r.(?) p.(Pro234Leu)
+/+ - c.715dup r.(?) p.(Tyr239LeufsTer50)
+/+ - c.724A>G r.(?) p.(Ser242Gly)
-/. - c.744G>A r.(?) p.(Thr248=)
-?/. - c.744G>A r.(?) p.(Thr248=)
+/+ - c.768C>A r.(?) p.(Asp256Glu)
+/+ - c.769del r.(?) p.(Gln257SerfsTer109)
-?/. - c.771G>A r.(?) p.(Gln257=)
+/+ - c.777dup r.(?) p.(Glu260ArgfsTer29)
-?/. - c.782C>T r.(?) p.(Pro261Leu)
-?/. - c.782C>T r.(?) p.(Pro261Leu)
-?/. - c.782C>T r.(?) p.(Pro261Leu)
-?/. - c.783G>A r.(?) p.(Pro261=)
-?/. - c.805G>A r.(?) p.(Ala269Thr)
+/+ - c.806del r.(?) p.(Ser269Phefs*9)
-/. - c.813A>G r.(?) p.(Thr271=)
+/+ - c.821del r.(?) p.(Gly274Aspfs*4)
+/+ - c.826G>T r.(?) p.(Asp276Tyr)
+/+ - c.831C>A r.(?) p.(Tyr277*)
-?/. - c.840C>A r.(?) p.(Ile280=)
-?/. - c.840C>A r.(?) p.(Ile280=)
-/- - c.840C>A r.(?) p.(Ile280=)
+/+ - c.845_852del r.(?) p.(Ser282AsnfsTer4)
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