Transcript #00002596 (NM_032208.2, ANTXR1 gene)

Transcript name transcript variant 1
Gene name ANTXR1 (anthrax toxin receptor 1)
Chromosome 2
Transcript - NCBI ID NM_032208.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_115584.1
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

75 entries on 1 page. Showing entries 1 - 75.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+/. - c.12_30dup r.(?) p.(Ile11GlyfsTer40)
+/. - c.12_30dup r.(?) p.(Ile11GlyfsTer40)
-?/. - c.18G>A r.(?) p.(Arg6=)
-/. - c.20G>A r.(?) p.(Arg7Lys)
?/. - c.34G>A r.(?) p.(Gly12Ser)
+/. - c.89dup r.(?) p.(Arg31ThrfsTer14)
+/. 1i c.152+1G>A r.spl p.?
+/. 1i c.152+2T>C r.spl p.?
+/. 1i c.152+2T>C r.spl p.?
+/. 1i c.152+3_152+6del r.spl p.?
+/. 1i c.152+3_152+6del r.spl p.?
+/. 2i_3i c.(224+1_225-1)_(296+1_297-1)del p.(Ser75_Asp98del) p.(Ser75_Asp98del)
+/. - c.262C>T r.(?) p.(Arg88*)
+/. - c.262C>T r.(?) p.(Arg88Ter)
+/. - c.262C>T r.(?) p.(Arg88Ter)
+/. - c.265G>A r.(?) p.(Gly89Arg)
?/. - c.292G>A r.(?) p.(Asp98Asn)
?/. 3i_6i c.(296+1_297-1)_(492+1_493-1)del r.(?) p.(Glu100LeufsTer16)
-?/. - c.373G>C r.(?) p.(Glu125Gln)
+/. 4i c.378+3A>G r.spl p.?
+?/. - c.379-2del r.spl? p.?
+/. - c.410A>T r.(?) p.(Gln137Leu)
+/. - c.410A>T r.(?) p.(Gln137Leu)
+/. 5 c.411A>G r.spl p.?
+/. 5 c.411A>G r.spl p.?
+/. 5 c.411A>G r.spl p.?
?/. - c.430G>A r.(?) p.(Val144Ile)
-/. - c.450T>C r.(?) p.(Asp150=)
-/. - c.492+10G>A r.(=) p.(=)
+/. - c.505C>T r.(?) p.(Arg169Ter)
-?/. - c.561+7T>C r.(=) p.(=)
?/. - c.568del r.(?) p.(Arg190GlyfsTer12)
?/. - c.623T>C r.(?) p.(Leu208Pro)
+/. - c.664G>A r.(?) p.(Glu222Lys)
+/. - c.664G>A r.(?) p.(Glu222Lys)
-?/. - c.720C>T r.(?) p.(Val240=)
?/. - c.748C>T r.(?) p.(Arg250Cys)
?/. - c.754G>A r.(?) p.(Val252Met)
?/. - c.781A>G r.(?) p.(Ile261Val)
-?/. - c.849G>A r.(?) p.(Ala283=)
-?/. - c.901G>A r.(?) p.(Asp301Asn)
+/. - c.949T>C r.(?) p.(Cys317Arg)
+/. - c.949T>C r.(?) p.(Cys317Arg)
-?/. - c.975C>T r.(?) p.(Ile325=)
+?/. 13 c.976G>A r.976G>A p.Ala326Thr
?/. - c.976G>A r.(?) p.(Ala326Thr)
-?/. - c.978C>T r.(?) p.(Ala326=)
?/. - c.1031C>G r.(?) p.(Pro344Arg)
?/. - c.1073C>T r.(?) p.(Pro358Leu)
?/. - c.1099G>T r.(?) p.(Asp367Tyr)
-?/. - c.1131G>A r.(?) p.(Thr377=)
+/. - c.1150G>A r.(?) p.(Gly384Ser)
+/. - c.1150G>A r.(?) p.(Gly384Ser)
+/. - c.1150G>A r.(?) p.(Gly384Ser)
-/. - c.1185+16C>A r.(=) p.(=)
?/. - c.1190G>A r.(?) p.(Arg397His)
+/. - c.1221dup r.(?) p.(Ala408CysfsTer2)
-?/. - c.1224T>G r.(?) p.(Ala408=)
-?/. - c.1245T>C r.(?) p.(Asn415=)
?/. - c.1305_1307del r.(?) p.(Asn436del)
?/. - c.1305_1307del r.(?) p.(Asn436del)
?/. - c.1312C>T r.(?) p.(Arg438Cys)
+/. - c.1312C>T r.(?) p.(Arg438Cys)
-?/. - c.1368C>T r.(?) p.(Ala456=)
?/. - c.1433C>T r.(?) p.(Thr478Met)
-?/. - c.1434+9C>T r.(=) p.(=)
-?/. - c.1434+9C>T r.(=) p.(=)
+/. 17i c.1435-12A>G r.(1434_1435ins1435-11_1435-1) p.(Gly479PhefsTer119)
+/. 17i c.1435-2A>T r.spl p.?
+/. 17i c.1435-2A>T r.spl p.?
+?/. - c.1488dup r.(?) p.(Leu497Thrfs*86)
-?/. - c.1517C>T r.(?) p.(Pro506Leu)
?/. - c.1534del r.(?) p.(Tyr512Thrfs*82)
-?/. - c.1553C>T r.(?) p.(Ala518Val)
-/. - c.1554G>A r.(?) p.(Ala518=)
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