Transcript #00022572 (NM_004385.4, VCAN gene)

Transcript name transcript variant 1
Gene name VCAN (versican)
Chromosome 5
Transcript - NCBI ID NM_004385.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_004376.2
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

251 entries on 3 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. _1 c.-648A>G r.(=) p.(=)
?/. - c.58G>A r.(?) p.(Ala20Thr)
-?/. - c.70+12A>G r.(=) p.(=)
-/. - c.71-18A>G r.(=) p.(=)
-?/. - c.92C>T r.(?) p.(Pro31Leu)
-?/. - c.157C>T r.(?) p.(Pro53Ser)
?/. - c.170A>C r.(?) p.(Asn57Thr)
?/. - c.237A>T r.(?) p.(Lys79Asn)
-?/. - c.249C>A r.(?) p.(Val83=)
?/. - c.329T>G r.(?) p.(Val110Gly)
-/. - c.348T>C r.(?) p.(Thr116=)
-/. - c.393C>T r.(?) p.(Asp131=)
-/. - c.426G>A r.(?) p.(=)
-?/. - c.468G>A r.(?) p.(Ala156=)
-?/. - c.522C>T r.(?) p.(Asp174=)
-?/. - c.574G>A r.(?) p.(Gly192Arg)
-?/. - c.574G>A r.(?) p.(Gly192Arg)
-?/. - c.574G>A r.(?) p.(Gly192Arg)
-?/. - c.574G>A r.(?) p.(Gly192Arg)
-?/. - c.634G>A r.(?) p.(Ala212Thr)
-/. - c.645A>G r.(?) p.(Val215=)
-?/. - c.749-9T>C r.(=) p.(=)
-/. - c.763C>T r.(?) p.(Leu255Phe)
?/. - c.775_786del r.(?) p.(Ser259_Thr262del)
?/. - c.854C>T r.(?) p.(Ala285Val)
-/. - c.888C>T r.(?) p.(Tyr296=)
-/. - c.899C>T r.(?) p.(Ser300Leu)
-?/. - c.927T>C r.(?) p.(Thr309=)
?/. - c.1042C>T r.(?) p.(Pro348Ser)
-/. - c.1043-10A>G r.(=) p.(=)
-/. - c.1045A>G r.(?) p.(Lys349Glu)
-/. - c.1045A>G r.(?) p.(Lys349Glu)
-/. - c.1045A>G r.(?) p.(Lys349Glu)
-?/. - c.1127A>C r.(?) p.(Asp376Ala)
-?/. - c.1191C>T r.(?) p.(Pro397=)
-?/. - c.1192G>A r.(?) p.(Val398Met)
-/. - c.1227A>G r.(?) p.(Thr409=)
-/. - c.1243A>G r.(?) p.(Ile415Val)
-?/. - c.1243A>G r.(?) p.(Ile415Val)
-?/. - c.1251T>C r.(?) p.(Asp417=)
-?/. - c.1281T>C r.(?) p.(Thr427=)
-/. - c.1283G>A r.(?) p.(Gly428Asp)
-/. - c.1283G>A r.(?) p.(Gly428Asp)
-?/. - c.1371A>G r.(?) p.(=)
-?/. - c.1395C>T r.(?) p.(Gly465=)
-?/. - c.1400C>T r.(?) p.(Ser467Phe)
-/. - c.1400C>T r.(?) p.(Ser467Phe)
-/. - c.1521C>T r.(?) p.(His507=)
-?/. - c.1523T>A r.(?) p.(Ile508Asn)
-?/. - c.1523T>A r.(?) p.(Ile508Asn)
-/. - c.1523T>A r.(?) p.(Ile508Asn)
-?/. - c.1571G>A r.(?) p.(Arg524Lys)
-?/. - c.1571G>C r.(?) p.(Arg524Thr)
-?/. - c.1831A>G r.(?) p.(Met611Val)
-/. - c.1864T>C r.(?) p.(Trp622Arg)
-?/. - c.1895C>A r.(?) p.(Thr632Lys)
-/. - c.1895C>T r.(?) p.(Thr632Met)
-/. - c.1895C>T r.(?) p.(Thr632Met)
?/. - c.1895C>T r.(?) p.(Thr632Met)
?/. - c.1931C>T r.(?) p.(Pro644Leu)
?/. - c.1931C>T r.(?) p.(Pro644Leu)
-/. - c.2028A>G r.(?) p.(Leu676=)
-?/. - c.2028A>G r.(?) p.(Leu676=)
-/. - c.2065A>G r.(?) p.(Thr689Ala)
?/. - c.2101G>A r.(?) p.(Asp701Asn)
?/. 7 c.2104G>A r.(?) p.(Glu702Lys)
?/. - c.2125A>G r.(?) p.(Lys709Glu)
-?/. - c.2159T>C r.(?) p.(Val720Ala)
-?/. - c.2180C>G r.(?) p.(Ser727Cys)
-/. - c.2220T>C r.(?) p.(Ser740=)
?/. - c.2234A>C r.(?) p.(Lys745Thr)
?/. - c.2234A>C r.(?) p.(Lys745Thr)
?/. - c.2338G>T r.(?) p.(Asp780Tyr)
-/. - c.2378T>C r.(?) p.(Leu793Ser)
?/. - c.2656A>G r.(?) p.(Thr886Ala)
-?/. - c.2666C>T r.(?) p.(Thr889Ile)
-/. - c.2666C>T r.(?) p.(Thr889Ile)
-?/. - c.2784A>G r.(?) p.(Val928=)
-?/. - c.2784A>G r.(?) p.(Val928=)
-?/. - c.2875A>T r.(?) p.(Ser959Cys)
-/. - c.2887C>T r.(?) p.(Pro963Ser)
-/. - c.2887C>T r.(?) p.(Pro963Ser)
-/. - c.2887C>T r.(?) p.(Pro963Ser)
?/. - c.2891C>T r.(?) p.(Thr964Ile)
-?/. - c.2895T>G r.(?) p.(Thr965=)
-?/. - c.3076A>G r.(?) p.(Ile1026Val)
-?/. - c.3076A>G r.(?) p.(Ile1026Val)
-/. - c.3094C>G r.(?) p.(Gln1032Glu)
-?/. - c.3188T>C r.(?) p.(Leu1063Pro)
?/. - c.3192T>A r.(?) p.(Asp1064Glu)
-/. - c.3201G>A r.(?) p.(Glu1067=)
?/. - c.3205G>A r.(?) p.(Asp1069Asn)
+/. 7 c.3455C>A r.(?) p.(Ser1152*)
-?/. - c.3528G>A r.(?) p.(Glu1176=)
-?/. - c.3531T>C r.(?) p.(Asp1177=)
-/. - c.3639A>G r.(?) p.(Ser1213=)
?/. - c.3749T>G r.(?) p.(Ile1250Ser)
-?/. - c.3933G>A r.(?) p.(Gln1311=)
?/. - c.3959C>T r.(?) p.(Pro1320Leu)
-/. - c.4003+16C>G r.(=) p.(=)
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