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QuickView for rs149858549;jsessionid=22A7CB786A35AB5D2D6F42D429061FFF (snp)


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      • Human Human A|G
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Type:
SNP
Organism:
Homo sapiens
Alleles:
A|G
Chromosomal Location:
chr 14 : 99863338 (build 36.3)
Strand:
+
Update Date:
Nov 14 2011
Associated Gene(s):
SLC25A47
Related URLs:
NCBI dbSNP


SLC25A47   (exon)  QuickView

Transcript CDS Change Protein Mutation Class AA Change
NM_207117
G205A NP_997000 Missense V69M