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QuickView for rs138240804;jsessionid=C640E5D7E238A4FF34C6FF453D154686 (snp)


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      • Human Human C|G
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Type:
SNP
Organism:
Homo sapiens
Alleles:
C|G
Chromosomal Location:
chr 7 : 34817915 (build 36.3)
Strand:
+
Update Date:
Nov 14 2011
Associated Gene(s):
NPSR1
Related URLs:
NCBI dbSNP


NPSR1   (exon)  QuickView

Transcript CDS Change Protein Mutation Class AA Change
NM_207172
G393C NP_997055 Synonymous L131L
NM_207173
G393C NP_997056 Synonymous L131L