Correlation Engine 2.0
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QuickView for rs143769498;jsessionid=B3AFF9AD95A979F7B8526D5D8F9D0AF6 (snp)


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      • Human Human C|G
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Type:
SNP
Organism:
Homo sapiens
Alleles:
C|G
Chromosomal Location:
chr 15 : 61232965 (build 36.3)
Strand:
+
Update Date:
Nov 14 2011
Associated Gene(s):
RPS27L
Related URLs:
NCBI dbSNP


RPS27L   (UTR)  QuickView

Transcript CDS Change Protein Mutation Class AA Change
NM_015920
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