Transcript #00025852 (NM_001318852.2, MAPK8IP3 gene)

Transcript name transcript variant 3
Gene name MAPK8IP3 (mitogen-activated protein kinase 8 interacting protein 3)
Chromosome 16
Transcript - NCBI ID NM_001318852.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_001305781.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2023-09-01 10:34:24 +02:00 (CEST)
Date last edited N/A


Variants

59 entries on 1 page. Showing entries 1 - 59.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/. - c.44A>G r.(?) p.(Tyr15Cys)
+/. - c.65del r.(?) p.(Gly22AlafsTer3)
+/. - c.79G>T r.(?) p.(Glu27Ter)
+/. - c.111C>G r.(?) p.(Tyr37Ter)
?/. - c.496C>T r.(?) p.(Gln166*)
-?/. - c.602+7_602+56del r.(=) p.(=)
-?/. - c.602+21_602+45del r.(=) p.(=)
-?/. - c.653C>G r.(?) p.(Thr218Arg)
?/. - c.659G>A r.(?) p.(Arg220His)
?/. - c.848C>T r.(?) p.(Ser283Leu)
-?/. - c.1185C>T r.(?) p.(Ile395=)
+/. - c.1201G>A r.(?) p.(Gly401Arg)
-?/. - c.1216+682G>A r.(=) p.(=)
-?/. - c.1217-5G>A r.spl? p.?
+/. - c.1334T>C r.(?) p.(Leu445Pro)
+/. - c.1334T>C r.(?) p.(Leu445Pro)
-?/. - c.1427G>A r.(?) p.(Arg476His)
-?/. - c.1458-3_1458-2del r.spl? p.?
?/. - c.1567C>T r.(?) p.(Arg523Cys)
+/. - c.1577G>A r.(?) p.(Arg526Gln)
+/. - c.1735C>T r.(?) p.(Arg579Cys)
+/. - c.1735C>T r.(?) p.(Arg579Cys)
+/. - c.1735C>T r.(?) p.(Arg579Cys)
+/. - c.1735C>T r.(?) p.(Arg579Cys)
+/. - c.1735C>T r.(?) p.(Arg579Cys)
-?/. - c.1758C>T r.(?) p.(Ser586=)
?/. - c.1910C>T r.(?) p.(Ser637Phe)
?/. - c.1936G>A r.(?) p.(Glu646Lys)
+?/. - c.2121+1dup r.spl p.(Leu708Alafs*16)
?/. - c.2254G>A r.(?) p.(Ala752Thr)
-?/. - c.2278_2280del r.(?) p.(Lys760del)
-?/. - c.2373C>T r.(?) p.(Ala791=)
?/. - c.2416G>A r.(?) p.(Ala806Thr)
-?/. - c.2446G>C r.(?) p.(Ala816Pro)
?/. - c.2473G>A r.(?) p.(Gly825Arg)
-?/. - c.2842A>G r.(?) p.(Ser948Gly)
?/. - c.2865_2870del r.(?) p.(Glu956_Pro957del)
-?/. - c.2868G>C r.(?) p.(Glu956Asp)
+/. - c.2985C>G r.(?) p.(His995Gln)
-?/. - c.3406C>T r.(?) p.(Leu1136=)
+/. - c.3439C>T r.(?) p.(Arg1147Cys)
+/. - c.3439C>T r.(?) p.(Arg1147Cys)
+/. - c.3439C>T r.(?) p.(Arg1147Cys)
+/. - c.3439C>T r.(?) p.(Arg1147Cys)
+/. - c.3439C>T r.(?) p.(Arg1147Cys)
+/. - c.3439C>T r.(?) p.(Arg1147Cys)
+/. - c.3439C>T r.(?) p.(Arg1147Cys)
+?/. - c.3440G>A r.(?) p.(Arg1147His)
?/. - c.3440G>A r.(?) p.(Arg1147His)
?/. - c.3440G>A r.(?) p.(Arg1147His)
?/. - c.3590A>T r.(?) p.(Glu1197Val)
-?/. - c.3598C>T r.(?) p.(Arg1200Cys)
?/. - c.3599G>A r.(?) p.(Arg1200His)
?/. - c.3604G>A r.(?) p.(Gly1202Arg)
-?/. - c.3604G>A r.(?) p.(Gly1202Arg)
-?/. - c.3826G>A r.(?) p.(Glu1276Lys)
?/. - c.3998C>T r.(?) p.(Ser1333Phe)
-?/. - c.4009G>A r.(?) p.(Glu1337Lys)
?/. - c.4009G>T r.(?) p.(Glu1337*)
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