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QuickView for rs112679001;jsessionid=1845A7328B4B6202092CA0352C204A27 (snp)


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Type:
SNP
Organism:
Homo sapiens
Alleles:
A|C
Chromosomal Location:
chr 11 : 65891575 (build 36.3)
Strand:
+
Update Date:
Nov 14 2011
Associated Gene(s):
SLC29A2
Related URLs:
NCBI dbSNP


SLC29A2   (exon)  QuickView

Transcript CDS Change Protein Mutation Class AA Change
NM_001532
G669T NP_001523 Synonymous L223L