Transcript #00007156 (NM_004431.3, EPHA2 gene)

Transcript name EPH receptor A2
Gene name EPHA2 (EPH receptor A2)
Chromosome 1
Transcript - NCBI ID NM_004431.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_004422.2
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

92 entries on 1 page. Showing entries 1 - 92.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.86-9C>T r.(=) p.(=)
-?/. - c.141G>A r.(?) p.(Pro47=)
-?/. - c.174C>A r.(?) p.(Ile58=)
?/. - c.410G>T r.(?) p.(Arg137Leu)
?/. - c.430A>G r.(?) p.(Thr144Ala)
?/. - c.437C>T r.(?) p.(Ala146Val)
-?/. - c.453C>T r.(?) p.(Thr151=)
?/. - c.523C>T r.(?) p.(Arg175Cys)
-/. - c.570G>A r.(?) p.(Ala190=)
-/. - c.573G>A r.(?) p.(Leu191=)
-?/. - c.648C>T r.(?) p.(Ala216=)
?/. - c.649G>C r.(?) p.(Gly217Arg)
-/. - c.695A>G r.(?) p.(Asp232Gly)
-?/. - c.714G>C r.(?) p.(Pro238=)
-?/. - c.741T>C r.(?) p.(Cys247=)
-/. - c.824-11G>A r.(=) p.(=)
-/. - c.824-11G>A r.(=) p.(=)
+?/. - c.944G>A r.(?) p.(Arg315Gln)
+?/. - c.983C>A r.(?) p.(Pro328His)
?/. - c.1048C>A r.(?) p.(Pro350Thr)
+/. 5 c.1059_1060dup r.(?) p.(Ser354Thrfs*40)
-?/. - c.1061G>A r.(?) p.(Ser354Asn)
?/. - c.1069C>T r.(?) p.(Arg357Cys)
?/. - c.1180C>T r.(?) p.(Arg394Cys)
-?/. - c.1312+6G>C r.(=) p.(=)
-?/. - c.1314G>A r.(?) p.(Glu438=)
+/. - c.1315C>T r.(?) p.(Pro439Ser)
+/. - c.1337dup r.(?) p.(Arg447Profs*7)
?/. - c.1360G>A r.(?) p.(Val454Ile)
-?/. - c.1362C>A r.(?) p.(Val454=)
-?/. - c.1383G>A r.(?) p.(Pro461=)
+/. - c.1405T>C r.(?) p.(Tyr469His)
?/. - c.1436C>T r.(?) p.(Ser479Phe)
-?/. - c.1512G>T r.(?) p.(=)
-?/. - c.1532C>T r.(?) p.(Thr511Met)
-?/. - c.1532C>T r.(?) p.(Thr511Met)
?/. - c.1532C>T r.(?) p.(Thr511Met)
-?/. - c.1532C>T r.(?) p.(Thr511Met)
+?/. - c.1543C>T r.(?) p.(Gln515Ter)
?/. - c.1552G>A r.(?) p.(Gly518Ser)
+?/. - c.1582+2T>G r.spl? p.?
+/. - c.1751C>T r.(?) p.(Pro584Leu)
+/. - c.1751C>T r.(?) p.(Pro584Leu)
+?/. - c.1751C>T r.(?) p.(Pro584Leu)
+?/. - c.1751C>T r.(?) p.(Pro584Leu)
+/. - c.1751C>T r.(?) p.(Pro584Leu)
-?/. - c.1776C>T r.(?) p.(His592=)
-?/. - c.1813A>G r.(?) p.(Thr605Ala)
?/. - c.1814C>T r.(?) p.(Thr605Ile)
?/. - c.1814C>T r.(?) p.(Thr605Ile)
?/. - c.1844G>A r.(?) p.(Arg615Gln)
-?/. - c.1857C>T r.(?) p.(Ile619=)
-?/. - c.1896G>A r.(?) p.(Leu632=)
-?/. - c.1941G>T r.(?) p.(Thr647=)
?/. - c.1978T>G r.(?) p.(Phe660Val)
-?/. - c.1983C>T r.(?) p.(Leu661=)
-?/. - c.1984G>A r.(?) p.(Gly662Ser)
-?/. - c.1986C>G r.(?) p.(Gly662=)
+/. - c.2007G>T r.(?) p.(Gln669His)
-?/. - c.2094G>A r.(?) p.(Gly698=)
?/. - c.2162G>A r.(?) p.(Arg721Gln)
?/. - c.2162G>A r.(?) p.(Arg721Gln)
-?/. - c.2169C>T r.(?) p.(Ile723=)
?/. - c.2239G>A r.(?) p.(Val747Ile)
+?/. - c.2439T>G r.(?) p.(Tyr813Ter)
?/. - c.2581C>T r.(?) p.(Arg861Cys)
-?/. - c.2627G>A r.(?) p.(Arg876His)
?/. - c.2671G>C r.(?) p.(Val891Leu)
-?/. - c.2700C>G r.(?) p.(Gly900=)
?/. - c.2800G>A r.(?) p.(Glu934Lys)
+/. - c.2803A>T r.(?) p.(Lys935Ter)
+?/. - c.2819C>T r.(?) p.(Thr940Ile)
+?/. - c.2825+1G>A r.spl p.(?)
+?/. - c.2826-9G>A r.spl p.?
+?/. - c.2826-9G>A r.spl p.?
+?/. - c.2826-9G>A r.spl p.?
+?/. - c.2826-9G>A r.spl p.?
+?/. - c.2826-9G>A r.spl p.?
+?/. - c.2826-9G>A r.spl p.?
+?/. - c.2826-9G>A r.spl p.?
+/. 16i c.2826-9G>A r.spl p.?
+?/. - c.2826-9G>A r.spl p.?
+/. 16i c.2826-9G>A r.spl p.?
+?/. - c.2826-9G>A r.spl? p.(?)
+/. - c.2826-9G>A r.(=) p.(=)
+?/. - c.2842G>A r.(?) p.(Gly948Arg)
+?/. 17 c.2870G>C r.(?) p.(Arg957Pro)
-?/. - c.2874C>T r.(?) p.(Ile958=)
-/. - c.2874C>T r.(?) p.(Ile958=)
?/. - c.2875G>A r.(?) p.(Ala959Thr)
-?/. - c.2904G>C r.(?) p.(Gln968His)
-/. - c.2919G>A r.(?) p.(Gly973=)
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