Correlation Engine 2.0
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QuickView for rs111465454;jsessionid=7606CD0AE138C1012EAA017FEE10C3B4 (snp)


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      • Human Human G|C
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Type:
SNP
Organism:
Homo sapiens
Alleles:
G|C
Chromosomal Location:
chr 14 : 33463975 (build 36.3)
Strand:
+
Update Date:
Nov 14 2011
Associated Gene(s):
EGLN3
Related URLs:
NCBI dbSNP


EGLN3   (UTR)  QuickView

Transcript CDS Change Protein Mutation Class AA Change
NM_022073
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