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QuickView for rs149874318;jsessionid=B448E770B3E5F0732588221F4AE5F957 (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 : 112800526 (build 36.3)
Strand:
+
Update Date:
Nov 14 2011
Associated Gene(s):
DRD2
Related URLs:
NCBI dbSNP


DRD2   (exon)  QuickView

Transcript CDS Change Protein Mutation Class AA Change
NM_000795
C58T NP_000786 Missense R20W
NM_016574
C58T NP_057658 Missense R20W