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QuickView for rs148392548;jsessionid=53E65A1E33FF08F5806476371AEA49CF (snp)


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      • Human Human A|G
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Type:
SNP
Organism:
Homo sapiens
Alleles:
A|G
Chromosomal Location:
chr 7 : 73289640 (build 36.3)
Strand:
+
Update Date:
Nov 14 2011
Associated Gene(s):
RFC2
Related URLs:
NCBI dbSNP


RFC2   (exon)  QuickView

Transcript CDS Change Protein Mutation Class AA Change
NM_002914
C726T NP_002905 Synonymous D242D
NM_181471
C828T NP_852136 Synonymous D276D