Transcript #00000028 (NM_005529.5, HSPG2 gene)

Transcript name heparan sulfate proteoglycan 2
Gene name HSPG2 (heparan sulfate proteoglycan 2)
Chromosome 1
Transcript - NCBI ID NM_005529.5
Transcript - Ensembl ID -
Protein - NCBI ID NP_005520.4
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2012-05-11 13:11:52 +02:00 (CEST)
Date last edited N/A


Variants

485 entries on 5 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
./. - c.-626700_*1609068del r.? p.?
-?/. - c.109G>A r.(?) p.(Asp37Asn)
-?/. - c.204C>A r.(?) p.(Asp68Glu)
-?/. - c.204C>A r.(?) p.(Asp68Glu)
?/. - c.257C>G r.(?) p.(Ala86Gly)
-/. - c.324C>T r.(?) p.(Phe108=)
-?/. - c.325C>G r.(?) p.(Arg109Gly)
-?/. - c.337G>A r.(?) p.(Glu113Lys)
?/. - c.337G>A r.(?) p.(Glu113Lys)
-?/. - c.392T>C r.(?) p.(Val131Ala)
?/. - c.415G>T r.(?) p.(Glu139Ter)
?/. - c.416A>T r.(?) p.(Glu139Val)
-/. - c.444G>C r.(?) p.(Leu148=)
-?/. - c.467C>T r.(?) p.(Ala156Val)
?/. - c.470A>G r.(?) p.(Asp157Gly)
-/. - c.474G>T r.(?) p.(Gly158=)
-?/. - c.598A>T r.(?) p.(Thr200Ser)
-?/. - c.662G>A r.(?) p.(Arg221Gln)
?/. - c.670G>A r.(?) p.(Asp224Asn)
-?/. - c.732A>G r.(?) p.(Thr244=)
-?/. - c.732A>G r.(?) p.(Thr244=)
-?/. - c.745G>A r.(?) p.(Val249Met)
?/. - c.811G>A r.(?) p.(Ala271Thr)
+?/. - c.862del r.(?) p.(Gln288Argfs*30)
?/. - c.877C>T r.(?) p.(Arg293Cys)
-?/. - c.901G>A r.(?) p.(Asp301Asn)
?/. - c.907C>T r.(?) p.(Leu303Phe)
?/. - c.913G>A r.(?) p.(Asp305Asn)
-?/. - c.959-5C>T r.spl? p.?
?/. - c.1048T>C r.(?) p.(Cys350Arg)
-?/. - c.1082C>A r.(?) p.(Thr361Asn)
?/. - c.1082C>A r.(?) p.(Thr361Asn)
?/. - c.1123T>C r.(?) p.(Cys375Arg)
?/. - c.1187A>C r.(?) p.(Asp396Ala)
?/. - c.1187A>C r.(?) p.(Asp396Ala)
-?/. - c.1238G>A r.(?) p.(Arg413Gln)
-?/. - c.1238G>A r.(?) p.(Arg413Gln)
-?/. - c.1238G>A r.(?) p.(Arg413Gln)
-?/. - c.1259G>A r.(?) p.(Arg420Gln)
+/. - c.1267_1270del r.(?) p.(Thr423Ter)
?/. - c.1371C>A r.(?) p.(Ser457Arg)
-?/. - c.1450G>A r.(?) p.(Ala484Thr)
-?/. - c.1454G>A r.(?) p.(Arg485Gln)
-?/. - c.1480G>A r.(?) p.(Gly494Ser)
-?/. - c.1557G>A r.(?) p.(Leu519=)
-?/. - c.1557G>A r.(?) p.(Leu519=)
-?/. - c.1603C>T r.(?) p.(Arg535Cys)
-?/. 13 c.1627C>T r.(?) p.(Arg543Cys)
?/. - c.1628G>A r.(?) p.(Arg543His)
+/. - c.1654+15G>A r.spl? p.?
-?/. - c.1707G>C r.(?) p.(Thr569=)
-/. - c.1818+15_1818+27del r.(=) p.(=)
?/. - c.1843C>T r.(?) p.(Arg615Cys)
-?/. - c.1852G>A r.(?) p.(Val618Met)
?/. - c.1903G>A r.(?) p.(Val635Met)
?/. - c.1903G>A r.(?) p.(Val635Met)
-/. - c.1912A>G r.(?) p.(Met638Val)
?/. - c.1933C>T r.(?) p.(Leu645Phe)
+/. - c.1939C>T r.(?) p.(Arg647Ter)
+?/. - c.1940G>A r.(?) p.(Arg647Gln)
-?/. - c.1998+9C>T r.(=) p.(=)
-?/. - c.1998+9C>T r.(=) p.(=)
-?/. - c.1999-13C>T r.(=) p.(=)
?/. - c.2027C>T r.(?) p.(Pro676Leu)
-?/. - c.2049G>A r.(?) p.(Leu683=)
-?/. 16 c.2074G>A r.(?) p.(Val692Met)
?/. - c.2074G>A r.(?) p.(Val692Met)
-?/. - c.2074G>A r.(?) p.(Val692Met)
-?/. - c.2074G>A r.(?) p.(Val692Met)
?/. - c.2092T>C r.(?) p.(Tyr698His)
-/. - c.2109C>T r.(?) p.(Ala703=)
+?/. - c.2195+1G>T r.spl? p.?
-?/. - c.2260G>A r.(?) p.(Gly754Ser)
-/. - c.2294A>G r.(?) p.(Asn765Ser)
-?/. - c.2335C>T r.(?) p.(His779Tyr)
?/. - c.2335C>T r.(?) p.(His779Tyr)
?/. - c.2343G>A r.(?) p.(=)
-?/. - c.2357A>G r.(?) p.(Asn786Ser)
./. - c.2357A>G r.(?) p.(Asn786Ser)
?/. - c.2357A>G r.(?) p.(Asn786Ser)
-?/. - c.2462C>T r.(?) p.(Ala821Val)
?/. - c.2467C>T r.(?) p.(Arg823Cys)
?/. - c.2467C>T r.(?) p.(Arg823Cys)
?/. - c.2521G>T r.(?) p.(Ala841Ser)
-?/. - c.2549G>A r.(?) p.(Arg850His)
-?/. - c.2558+9G>A r.(=) p.(=)
-?/. - c.2596G>A r.(?) p.(Gly866Ser)
-?/. - c.2628T>A r.(?) p.(Ile876=)
?/. - c.2633G>A r.(?) p.(Arg878His)
-?/. - c.2685+8T>G r.(=) p.(=)
?/. - c.2725G>A r.(?) p.(Gly909Ser)
-?/. - c.2755G>A r.(?) p.(Asp919Asn)
-?/. - c.2850T>C r.(?) p.(Pro950=)
-?/. - c.2869A>C r.(?) p.(Asn957His)
?/. - c.2890A>T r.(?) p.(Thr964Ser)
-?/. - c.2890A>T r.(?) p.(Thr964Ser)
?/. - c.2966A>G r.(?) p.(Tyr989Cys)
?/. - c.2987G>A r.(?) p.(Arg996His)
?/. - c.2998G>A r.(?) p.(Asp1000Asn)
?/. - c.3029G>A r.(?) p.(Arg1010His)
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