Correlation Engine 2.0
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QuickView for rs77107801;jsessionid=232FC4CE83032604F5B984A835E2EFE7 (snp)


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      • Human Human T|C
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Type:
SNP
Organism:
Homo sapiens
Alleles:
T|C
Chromosomal Location:
chr 12 : 123375981 (build 36.3)
Strand:
+
Update Date:
Nov 14 2011
Associated Gene(s):
NCOR2
Related URLs:
NCBI dbSNP


NCOR2   (exon)  QuickView

Transcript CDS Change Protein Mutation Class AA Change
NM_001077261
G7300A NP_001070729 Missense A2434T
NM_006312
G7486A NP_006303 Missense A2496T