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QuickView for rs111831728;jsessionid=08BCA638BB1D352BEBE1186695B51160 (snp)


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Type:
SNP
Organism:
Homo sapiens
Alleles:
T|C
Chromosomal Location:
chr 11 : 77509855 (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
A382G NP_001007028 Missense I128V
NM_024079
A382G NP_076984 Missense I128V