Transcript #00006904 (NM_016938.4, EFEMP2 gene)

Transcript name transcript variant 1
Gene name EFEMP2 (EGF containing fibulin-like extracellular matrix protein 2)
Chromosome 11
Transcript - NCBI ID NM_016938.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_058634.4
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

83 entries on 1 page. Showing entries 1 - 83.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-/. - c.-58G>A r.(?) p.(=)
?/. - c.14C>A r.(?) p.(Ala5Asp)
-?/. - c.27C>G r.(?) p.(Pro9=)
-?/. - c.27C>G r.(?) p.(Pro9=)
-?/. - c.34C>T r.(?) p.(Leu12=)
-?/. - c.96G>A r.(?) p.(Glu32=)
-?/. - c.99C>T r.(?) p.(Pro33=)
+/. - c.111+1G>A r.spl p.?
-?/. - c.111+102G>A r.(=) p.(=)
-/. - c.138C>T r.(?) p.(Asp46=)
-?/. - c.139C>T r.(?) p.(Pro47Ser)
-?/. - c.139C>T r.(?) p.(Pro47Ser)
-?/. - c.139C>T r.(?) p.(Pro47Ser)
-?/. - c.160+17G>T r.(=) p.(=)
-/. - c.161-10C>T r.(=) p.(=)
?/. - c.209A>G r.(?) p.(Lys70Arg)
-/. - c.276C>T r.(?) p.(His92=)
-/. - c.276C>T r.(?) p.(His92=)
-/. - c.276C>T r.(?) p.(His92=)
-/. - c.277G>A r.(?) p.(Gly93Ser)
-?/. - c.277G>A r.(?) p.(Gly93Ser)
-?/. - c.277G>A r.(?) p.(Gly93Ser)
-?/. - c.290C>T r.(?) p.(Pro97Leu)
-?/. - c.307G>A r.(?) p.(Ala103Thr)
?/. - c.339T>G r.(?) p.(Tyr113*)
-/. - c.367+90del r.(=) p.(=)
-?/. - c.367+187G>A r.(=) p.(=)
-?/. - c.368-11G>A r.(=) p.(=)
-?/. - c.368-11G>A r.(=) p.(=)
-?/. - c.368-4G>A r.spl? p.?
-?/. - c.368-4G>A r.spl? p.?
-?/. - c.368-4G>A r.spl? p.?
-?/. - c.368-4G>A r.spl? p.?
?/. - c.397G>A r.(?) p.(Asp133Asn)
+/. - c.481G>A r.(?) p.(Glu161Lys)
-/. - c.490+23G>C r.(=) p.(=)
-/. - c.490+23G>C r.(=) p.(=)
-/. - c.491-28_491-22del r.(=) p.(=)
?/. - c.494T>C r.(?) p.(Ile165Thr)
?/. - c.505C>A r.(?) p.(Arg169Ser)
?/. - c.506G>A r.(?) p.(Arg169His)
+/. - c.506G>A r.(?) p.(Arg169His)
+/. - c.506G>A r.(?) p.(Arg169His)
?/. 6 c.554G>A r.(?) p.(Arg185His)
?/. - c.562T>G r.(?) p.(Cys188Gly)
-?/. - c.564C>T r.(?) p.(Cys188=)
-?/. - c.570G>A r.(?) p.(Pro190=)
-?/. - c.607+19A>G r.(=) p.(=)
-/. - c.608-38_608-36del r.(=) p.(=)
?/. - c.628G>A r.(?) p.(Gly210Arg)
-?/. - c.774C>T r.(?) p.(Cys258=)
-/. - c.775A>G r.(?) p.(Ile259Val)
-/. - c.775A>G r.(?) p.(Ile259Val)
-/. - c.775A>G r.(?) p.(Ile259Val)
-/. - c.775A>G r.(?) p.(Ile259Val)
?/. - c.790C>T r.(?) p.(Arg264Cys)
-?/. - c.792T>C r.(?) p.(Arg264=)
-/. - c.848-19C>T r.(=) p.(=)
-?/. - c.872C>T r.(?) p.(Ala291Val)
-?/. - c.885C>T r.(?) p.(Ser295=)
-?/. - c.885C>T r.(?) p.(Ser295=)
-?/. - c.885C>T r.(?) p.(Ser295=)
-?/. - c.923G>A r.(?) p.(Arg308His)
?/. - c.923G>A r.(?) p.(Arg308His)
?/. - c.934A>G r.(?) p.(Thr312Ala)
?/. - c.937A>G r.(?) p.(Asn313Asp)
?/. - c.937_939delinsGAT r.(?) p.(Asn313Asp)
-?/. - c.939C>T r.(?) p.(Asn313=)
-?/. - c.939C>T r.(?) p.(Asn313=)
-?/. - c.975-15C>T r.(=) p.(=)
-?/. - c.975-15C>T r.(=) p.(=)
-?/. - c.977G>A r.(?) p.(Arg326His)
-?/. - c.1047C>T r.(?) p.(Thr349=)
?/. - c.1061G>A r.(?) p.(Arg354Gln)
?/. - c.1065C>A r.(?) p.(Ser355Arg)
?/. - c.1065C>A r.(?) p.(Ser355Arg)
?/. - c.1065C>A r.(?) p.(Ser355Arg)
-?/. - c.1095G>A r.(?) p.(Ala365=)
-?/. - c.1170+17C>T r.(=) p.(=)
-?/. - c.1188C>T r.(?) p.(Ser396=)
-/. - c.1188C>T r.(?) p.(Ser396=)
-?/. - c.1188C>T r.(?) p.(Ser396=)
-?/. - c.*282C>T r.(=) p.(=)
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