Transcript #00000817 (NM_005045.3, RELN gene)

Transcript name transcript variant 1
Gene name RELN (reelin)
Chromosome 7
Transcript - NCBI ID NM_005045.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_005036.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2012-09-13 12:54:01 +02:00 (CEST)
Date last edited N/A


Variants

539 entries on 6 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.-18_-1dup r.(?) p.(=)
-/. - c.-15_-1dup r.(?) p.(=)
-/. - c.-15_-1dup r.(?) p.(=)
-/. - c.-12_-1del r.(?) p.(=)
-/. - c.-12_-1dup r.(?) p.(=)
-/. - c.-12_-1dup r.(?) p.(=)
-/. - c.-9_-1dup r.(?) p.(=)
-/. - c.-9_-1dup r.(?) p.(=)
-/. - c.-6_-1dup r.(?) p.(=)
-/. - c.-6_-1dup r.(?) p.(=)
-?/. - c.-3_-1del r.(?) p.(=)
?/. - c.-3_-1dup r.(?) p.(=)
-/. - c.-3_-1dup r.(?) p.(=)
-/. - c.-3_-1dup r.(?) p.(=)
-/. - c.26A>C r.(?) p.(Gln9Pro)
?/. - c.40G>A r.(?) p.(Ala14Thr)
?/. - c.52_63dup r.(?) p.(Gly18_Leu21dup)
-?/. - c.59C>A r.(?) p.(Thr20Lys)
-?/. - c.59C>T r.(?) p.(Thr20Met)
-?/. - c.65G>A r.(?) p.(Arg22Lys)
-?/. - c.77C>T r.(?) p.(Ala26Val)
?/. - c.77C>T r.(?) p.(Ala26Val)
-?/. - c.139G>A r.(?) p.(Glu47Lys)
./. - c.139G>A r.(?) p.(Glu47Lys)
?/. - c.139G>A r.(?) p.(Glu47Lys)
./. - c.139G>A r.(?) p.(Glu47Lys)
./. - c.139G>A r.(?) p.(Glu47Lys)
?/. - c.163G>A r.(?) p.(Val55Met)
?/. - c.227-7068A>G r.(=) p.(=)
?/. - c.227-7068A>G r.(=) p.(=)
-/. - c.227-17dup r.(=) p.(=)
-?/. - c.396C>T r.(?) p.(His132=)
?/. - c.425G>A r.(?) p.(Ser142Asn)
-/. - c.473+22C>T r.(=) p.(=)
-?/. - c.474-7T>C r.(=) p.(=)
-?/. - c.474-7T>C r.(=) p.(=)
?/. - c.490C>T r.(?) p.Arg164Trp
-/. - c.565C>T r.(?) p.(His189Tyr)
-?/. - c.576A>G r.(?) p.(Leu192=)
-?/. - c.577+7G>T r.(=) p.(=)
-?/. - c.577+9T>C r.(=) p.(=)
-/. - c.577+26T>C r.(=) p.(=)
-/. - c.578-3T>C r.spl? p.?
-/. - c.578-3T>C r.spl? p.?
-/. - c.578-3T>C r.spl? p.?
-?/. - c.596G>A r.(?) p.(Ser199Asn)
-?/. - c.621C>T r.(?) p.(Asp207=)
-/. - c.621C>T r.(?) p.(Asp207=)
?/. - c.688C>G r.(?) p.(Gln230Glu)
?/. - c.754A>G r.(?) p.(Ile252Val)
?/. - c.795A>G r.(?) p.(Gln265=)
-?/. - c.807G>T r.(?) p.(Gly269=)
-/. - c.831T>C r.(?) p.(Tyr277=)
?/. - c.877G>A r.(?) p.(Asp293Asn)
?/. - c.877G>A r.(?) p.(Asp293Asn)
-?/. - c.906C>T r.(?) p.(Ala302=)
-?/. - c.906C>T r.(?) p.(Ala302=)
-?/. - c.1001G>A r.(?) p.(Arg334His)
-?/. - c.1035A>G r.(?) p.(Leu345=)
?/. - c.1072G>A r.(?) p.(Val358Ile)
-/. - c.1075G>A r.(?) p.(Val359Ile)
?/. - c.1108G>C r.(?) p.(Gly370Arg)
?/. - c.1108G>C r.(?) p.(Gly370Arg)
?/. - c.1117C>A r.(?) p.(Leu373Ile)
?/. - c.1145A>G r.(?) p.(His382Arg)
?/. - c.1228G>A r.(?) p.(Asp410Asn)
?/. - c.1231C>A r.(?) p.(Leu411Ile)
?/? 11 c.1231C>A r.(?) p.(Leu411Ile)
?/. - c.1240G>A r.(?) p.(Glu414Lys)
-?/. - c.1290-3dup r.spl? p.?
-/. - c.1290-3dup r.spl? p.?
./. - c.1331C>T r.(?) p.(Thr444Met)
?/. - c.1336G>C r.(?) p.(Glu446Gln)
?/. - c.1336G>C r.(?) p.(Glu446Gln)
-?/. - c.1377G>A r.(?) p.(=)
-?/. - c.1382T>C r.(?) p.(Leu461Ser)
?/. - c.1394C>T r.(?) p.(Ser465Phe)
?/. - c.1400A>C r.(?) p.(Asp467Ala)
-?/. - c.1402A>C r.(?) p.(Thr468Pro)
?/. - c.1405A>C r.(?) p.(Thr469Pro)
-?/. - c.1442-8T>C r.(=) p.(=)
-?/. - c.1480A>G r.(?) p.(Ile494Val)
-?/. - c.1554+5A>G r.spl? p.?
?/. - c.1555G>C r.(?) p.(Val519Leu)
-?/. - c.1555G>T r.(?) p.(Val519Phe)
./. - c.1555G>T r.(?) p.(Val519Phe)
-/. - c.1596G>A r.(?) p.(Gln532=)
-/. - c.1596G>A r.(?) p.(Gln532=)
-?/. - c.1702A>G r.(?) p.(Met568Val)
?/. - c.1726A>G r.(?) p.(Ile576Val)
-/. - c.1776A>G r.(?) p.(Glu592=)
-/. - c.1776A>G r.(?) p.(Glu592=)
?/. - c.1790A>G r.(?) p.(His597Arg)
-/. - c.1799C>T r.(?) p.(Ser600Phe)
-/. - c.1799C>T r.(?) p.(Ser600Phe)
?/. - c.1799C>T r.(?) p.(Ser600Phe)
-?/. - c.1799C>T r.(?) p.(Ser600Phe)
-?/. - c.1824C>T r.(?) p.(Cys608=)
-/. - c.1824C>T r.(?) p.(Cys608=)
-/. - c.1888A>C r.(?) p.(Ser630Arg)
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