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QuickView for rs145803977;jsessionid=8EE30DB77E109622D094561C8DE5CAFC (snp)


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      • Human Human A|G
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Type:
SNP
Organism:
Homo sapiens
Alleles:
A|G
Chromosomal Location:
chr 14 : 51851169 (build 36.3)
Strand:
+
Update Date:
Nov 14 2011
Associated Gene(s):
PTGER2
Related URLs:
NCBI dbSNP


PTGER2   (promoter / exon)  QuickView

Transcript CDS Change Protein Mutation Class AA Change
NM_000956
G153A NP_000947 Synonymous R51R