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QuickView for rs113166818;jsessionid=A5429557E2B5CCAFCBE7B8FA290CE448 (snp)


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      • Human Human C|G
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Type:
SNP
Organism:
Homo sapiens
Alleles:
C|G
Chromosomal Location:
chr 22 : 34112893 (build 36.3)
Strand:
+
Update Date:
Nov 14 2011
Associated Gene(s):
HMOX1
Related URLs:
NCBI dbSNP


HMOX1   (exon)  QuickView

Transcript CDS Change Protein Mutation Class AA Change
NM_002133
G360C NP_002124 Missense E120D