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QuickView for rs150213168;jsessionid=23B87EBB4ED407B88729D76910680BB7 (snp)


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      • Human Human A|G
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Type:
SNP
Organism:
Homo sapiens
Alleles:
A|G
Chromosomal Location:
chr 11 : 77498252 (build 36.3)
Strand:
+
Update Date:
Nov 14 2011
Associated Gene(s):
ALG8
Related URLs:
NCBI dbSNP


ALG8   (exon)  QuickView

Transcript CDS Change Protein Mutation Class AA Change
NM_001007027
C922T NP_001007028 Missense P308S
NM_024079
C922T NP_076984 Missense P308S