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QuickView for rs148094314;jsessionid=17E40357DEB320207CE33A9C60E2A069 (snp)


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      • Human Human A|T
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Type:
SNP
Organism:
Homo sapiens
Alleles:
A|T
Chromosomal Location:
chr 13 : 102499791 (build 36.3)
Strand:
+
Update Date:
Nov 14 2011
Associated Gene(s):
SLC10A2
Related URLs:
NCBI dbSNP


SLC10A2   (exon)  QuickView

Transcript CDS Change Protein Mutation Class AA Change
NM_000452
A768T NP_000443 Synonymous R256R