Correlation Engine 2.0
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QuickView for rs151278910;jsessionid=50750D8AEAAE04EC96832DA2346F931C (snp)


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      • Human Human T|C
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Type:
SNP
Organism:
Homo sapiens
Alleles:
T|C
Chromosomal Location:
chr 2 : 55106930 (build 36.3)
Strand:
+
Update Date:
Nov 14 2011
Associated Gene(s):
RTN4
Related URLs:
NCBI dbSNP


RTN4   (exon)  QuickView

Transcript CDS Change Protein Mutation Class AA Change
NM_020532
A1809G NP_065393 Synonymous S603S
NM_207521
A1191G NP_997404 Synonymous S397S