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QuickView for rs146915707 (snp)


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      • Human Human C|G
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Type:
SNP
Organism:
Homo sapiens
Alleles:
C|G
Chromosomal Location:
chr 11 : 62503929 (build 36.3)
Strand:
+
Update Date:
Nov 14 2011
Associated Gene(s):
SLC22A6
Related URLs:
NCBI dbSNP, HapMap


SLC22A6   (exon)  QuickView

Transcript CDS Change Protein Mutation Class AA Change
NM_004790
C1105G NP_004781 Missense L369V
NM_153276
C1105G NP_695008 Missense L369V
NM_153277
C1105G NP_695009 Missense L369V
NM_153278
C1105G NP_695010 Missense L369V