Transcript #00024007 (NM_001077416.2, TMEM231 gene)

Transcript name transcript variant 1
Gene name TMEM231 (transmembrane protein 231)
Chromosome 16
Transcript - NCBI ID NM_001077416.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_001070884.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2015-01-17 17:10:07 +01:00 (CET)
Date last edited N/A


Variants

89 entries on 1 page. Showing entries 1 - 89.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+/. - c.2T>A r.(?) p.(Met1?)
+/. - c.2T>A r.(?) p.(Met1?)
+/. - c.2T>A r.(?) p.(Met1?)
?/. - c.27G>A r.(?) p.(Trp9*)
+?/. - c.38C>A r.(?) p.(Ser13*)
-?/. - c.48C>T r.(?) p.(Ala16=)
-?/. - c.48C>T r.(?) p.(Ala16=)
-/. - c.57G>C r.(?) p.(Arg19=)
+/. - c.62C>G r.(?) p.(Ser21Ter)
-?/. - c.69C>G r.(?) p.(Arg23=)
?/. - c.122C>T r.(?) p.(Ala41Val)
?/. - c.152C>T r.(?) p.(Pro51Leu)
-?/. - c.157C>T r.(?) p.(Arg53Cys)
?/. - c.191C>T r.(?) p.(Ser64Phe)
?/. - c.242C>G r.(?) p.(Ala81Gly)
+/. - c.248C>A r.(?) p.(Ser83Ter)
+?/. - c.248C>A r.(?) p.(Ser83*)
+?/. - c.248C>A r.(?) p.(Ser83Ter)
-?/. - c.271C>G r.(?) p.(Arg91Gly)
?/. - c.284C>T r.(?) p.(Ala95Val)
?/. - c.325G>C r.(?) p.(Glu109Gln)
-/. - c.336G>C r.(?) p.(Pro112=)
-?/. - c.393C>T r.(?) p.(Asp131=)
+?/. - c.400C>T r.(?) p.(Leu134Phe)
+?/. 1 c.406T>G r.(?) p.(Trp136Gly)
?/. - c.413C>T r.(?) p.(Thr138Met)
+/. - c.420dup r.(?) p.(Ala141ArgfsTer18)
-?/. - c.421G>A r.(?) p.(Ala141Thr)
-?/. - c.444T>C r.(?) p.(Asp148=)
?/. - c.458C>T r.(?) p.(Pro153Leu)
-?/. - c.468+13C>A r.(=) p.(=)
+/. - c.511T>G r.(?) p.(Leu171Val)
+/. - c.532C>G r.(?) p.(Pro178Ala)
-?/. - c.546G>A r.(?) p.(Thr182=)
-?/. - c.558C>T r.(?) p.(Leu186=)
?/. - c.559G>A r.(?) p.(Gly187Ser)
?/. - c.597+1G>A r.spl? p.?
-?/. - c.597+13G>A r.(=) p.(=)
?/. - c.629C>T r.(?) p.(Ala210Val)
-?/. - c.629C>T r.(?) p.(Ala210Val)
-?/. - c.630G>A r.(?) p.(Ala210=)
-?/. - c.708G>A r.(?) p.(Pro236=)
+/. - c.712G>A r.(?) p.(Asp238Asn)
+/. - c.712G>A r.(?) p.(Asp238Asn)
+/. - c.712G>A r.(?) p.(Asp238Asn)
+/. 3 c.712G>A r.(?) p.(Asp238Asn)
+/. 3 c.712G>A r.(?) p.(Asp238Asn)
+/. 3 c.712G>A r.(?) p.(Asp238Asn)
-?/. - c.741C>T r.(?) p.(Asn247=)
-/. - c.741+3A>G r.spl? p.?
-/. - c.741+8C>G r.(=) p.(=)
-/. - c.741+17T>A r.(=) p.(=)
-/. - c.741+17T>A r.(=) p.(=)
+/. 3i_4 c.742-1_752delinsAGTATCTGTGAC r.spl p.?
+?/. 3i_4i c.(741+1_742-1)_(823+1_824-1)del r.(?) p.(Ile248Leufs*5)
?/. - c.743T>C r.(?) p.(Ile248Thr)
+/. 4 c.784G>A r.(?) p.(Asp262Asn)
+?/. - c.784G>A r.(?) p.(Asp262Asn)
+?/. - c.784G>A r.(?) p.(Asp262Asn)
+?/. - c.784G>A r.(?) p.(Asp262Asn)
-?/. - c.790A>T r.(?) p.(Thr264Ser)
?/. - c.823+4A>G r.spl? p.?
?/. - c.869G>C r.(?) p.(Arg290Thr)
?/. - c.869G>C r.(?) p.(Arg290Thr)
-?/. - c.869G>C r.(?) p.(Arg290Thr)
-?/. - c.869G>C r.(?) p.(Arg290Thr)
-?/. - c.878A>G r.(?) p.(Asp293Gly)
+?/. 5 c.906C>G r.(?) p.(Ile302Met)
+/. - c.929+1A>G r.spl p.?
+?/. - c.930-1C>G r.spl p.(?)
+?/. - c.930-1C>G r.spl p.(?)
+?/. - c.930-1C>G r.spl p.(?)
?/. - c.949A>G r.(?) p.(Lys288Glu)
?/. - c.950A>C r.(?) p.(Glu317Ala)
?/. - c.950A>C r.(?) p.(Glu317Ala)
?/. - c.983G>C r.(?) p.(Ser328Thr)
?/. - c.1030G>A r.(?) p.(Val344Met)
-/. - c.1050G>A r.(?) p.(Val350=)
?/. - c.1086C>A r.(?) p.(Asp362Glu)
-?/. - c.1086C>A r.(?) p.(Asp362Glu)
?/. - c.1087T>G r.(?) p.(Leu363Val)
-?/. - c.1087T>G r.(?) p.(Leu363Val)
?/. - c.1103T>G r.(?) p.(Leu368Ter)
-/. - c.*8A>G r.(=) p.(=)
-/. - c.*55G>A r.(=) p.(=)
-?/. - c.*69A>T r.(=) p.(=)
+/. - g.18555_19148conNG_026383.1:g.2718_3301 r.(=) p.(=)
+/. - g.18555_19148conNG_026383.1:g.2718_3301 r.(=) p.(=)
+/. - g.18555_19148conNG_026383.1:g.2718_3301 r.(=) p.(=)
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