Transcript #00013738 (NM_002430.2, MN1 gene)

Transcript name meningioma (disrupted in balanced translocation) 1
Gene name MN1 (meningioma (disrupted in balanced translocation) 1)
Chromosome 22
Transcript - NCBI ID NM_002430.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_002421.3
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

88 entries on 1 page. Showing entries 1 - 88.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+/. _1_2_ c.-955_*2638[0] r.0 p.0
+/. _1_2_ c.-955_*2638[0] r.0 p.0
-?/. - c.56G>A r.(?) p.(Gly19Asp)
?/. - c.56G>A r.(?) p.(Gly19Asp)
-?/. - c.244G>A r.(?) p.(Gly82Arg)
?/. - c.368C>T r.(?) p.(Pro123Leu)
-?/. - c.464A>C r.(?) p.(His155Pro)
+/. 1 c.536del r.(?) p.(Ser179*)
-?/. - c.725G>A r.(?) p.(Gly242Glu)
?/. - c.803G>T r.(?) p.(Gly268Val)
+/. - c.820_826del r.(?) p.(Gly274Profs*47)
?/. - c.847G>T r.(?) p.(Val283Leu)
-?/. - c.873G>C r.(?) p.(Gln291His)
?/. - c.908_925del r.(?) p.(Pro303_Gln308del)
-?/. - c.927_929del r.(?) p.(Gln309del)
?/. - c.968T>C r.(?) p.(Met323Thr)
+/. 1 c.1091dup r.(?) p.(Pro365Thrfs*120)
+/. 1 c.1415C>A r.(?) p.(Ser472*)
?/. - c.1415C>A r.(?) p.(Ser472Ter)
?/. - c.1423G>C r.(?) p.(Gly475Arg)
?/. - c.1501C>T r.(?) p.(Pro501Ser)
-?/. - c.1596_1598del r.(?) p.(Gln550del)
-/. - c.1596_1598dup r.(?) p.(Gln550dup)
-/. - c.1596_1598dup r.(?) p.(Gln550dup)
?/. - c.1598_1599insGC r.(?) p.(Gln534Hisfs*25)
+?/. - c.1598_1599insGC r.(?) p.(Gln534Hisfs*25)
?/. - c.1598_1599insGCAAC r.(?) p.(Gln535Hisfs*25)
-?/. - c.1599_1600insG r.(?) p.(Gln534Alafs*26)
-?/. - c.1605G>A r.(?) p.(Gln535=)
-?/. - c.1605_1625del r.(?) p.(Gln544_Gln550del)
-?/. - c.1605_1625del r.(?) p.(Gln544_Gln550del)
?/. - c.1608_1619dup r.(?) p.(Gln547_Gln550dup)
-?/. - c.1620A>G r.(?) p.(Gln540=)
-?/. - c.1649_1651del r.(?) p.(Gln550del)
?/. - c.1777G>T r.(?) p.(Gly593Cys)
?/. - c.1900G>C r.(?) p.(Gly634Arg)
-?/. - c.2015C>T r.(?) p.(Ser672Leu)
?/. - c.2015C>T r.(?) p.(Ser672Leu)
-?/. - c.2015C>T r.(?) p.(Ser672Leu)
-?/. - c.2079C>T r.(?) p.(Pro693=)
?/. - c.2107G>A r.(?) p.(Gly703Arg)
?/. - c.2186G>C r.(?) p.(Arg729Pro)
-?/. - c.2256C>T r.(?) p.(Gly752=)
-/. - c.2349T>G r.(?) p.(Gly783=)
+/. - c.2464C>T r.(?) p.(Gln822*)
?/. - c.2678C>G r.(?) p.(Pro893Arg)
+?/. - c.2813del r.(?) p.(Gly938Alafs*16)
?/. - c.2903G>A r.(?) p.(Ser968Asn)
+?/. - c.2935C>T r.(?) p.(Gln979*)
?/. - c.3260G>A r.(?) p.(Arg1087His)
?/. - c.3344C>T r.(?) p.(Pro1115Leu)
?/. - c.3448A>T r.(?) p.(Ile1150Phe)
-?/. - c.3550G>C r.(?) p.(Glu1184Gln)
+?/. - c.3686_3698del r.(?) p.(Met1229Argfs*87)
?/. - c.3724_3726del r.(?) p.(Asp1242del)
+/. 1 c.3727_3731dup r.(?) p.(Leu1245Argfs*77)
?/. - c.3731C>T r.(?) p.(Thr1244Met)
+?/. - c.3744G>A r.(?) p.(Trp1248*)
+/. 1 c.3745G>T r.3745g>u p.Glu1249*
+/. 1 c.3778G>T r.(?) p.(Glu1260*)
+/. - c.3778G>T r.(?) p.(Glu1260Ter)
+/. 2 c.3817C>T r.(?) p.(Gln1273*)
+/. 2 c.3817C>T r.(?) p.(Gln1273*)
+/. 2 c.3817C>T r.(?) p.(Gln1273*)
+/. 2 c.3817C>T r.(?) p.(Gln1273*)
?/. - c.3819G>T r.(?) p.(Gln1273His)
+/. - c.3835C>T r.(?) p.(Gln1279*)
+/. 2 c.3839del r.(?) p.(Cys1280Serfs*40)
+/. - c.3846_3849del r.(?) p.(Val1283Thrfs*36)
+/. 2 c.3849_3850delinsA r.(?) p.(His1284Thrfs*36)
+/. 2 c.3870_3879dup r.3870_3879dup p.Ala1294*
+?/. - c.3883C>T r.(?) p.(Arg1295Ter)
+/. - c.3883C>T r.(?) p.(Arg1295*)
+/. 2 c.3883C>T r.(?) p.(Arg1295*)
+/. 2 c.3883C>T r.(?) p.(Arg1295*)
+/. 2 c.3883C>T r.(?) p.(Arg1295*)
+/. 2 c.3883C>T r.(?) p.(Arg1295*)
+/. 2 c.3883C>T r.(?) p.(Arg1295*)
+/. 2 c.3883C>T r.(?) p.(Arg1295*)
+/. 2 c.3883C>T r.(?) p.(Arg1295*)
+/. 2 c.3883C>T r.(?) p.(Arg1295*)
+/. 2 c.3883C>T r.(?) p.(Arg1295*)
?/. - c.3883C>T r.(?) p.(Arg1295*)
+/. 2 c.3893_3894dup r.(?) p.(Pro1299Cysfs*22)
+/. 2 c.3903G>A r.(?) p.(Trp1301*)
+/. 2 c.3903G>A r.3903g>a p.Trp1301*
+/. 2 c.3903G>A r.(?) p.(Trp1301*)
+/. 2 c.3926_3931delins(17) r.(?) p.(Ser1309*)
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