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QuickView for rs150437940;jsessionid=19FE0FEBB9BC41690110B3C188B712FF (snp)


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      • Human Human A|G
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Type:
SNP
Organism:
Homo sapiens
Alleles:
A|G
Chromosomal Location:
chr 22 : 18331220 (build 36.3)
Strand:
+
Update Date:
Nov 14 2011
Associated Gene(s):
COMT
Related URLs:
NCBI dbSNP


COMT   (exon)  QuickView

Transcript CDS Change Protein Mutation Class AA Change
NM_000754
A421G NP_000745 Missense I141V
NM_007310
A271G NP_009294 Missense I91V