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QuickView for rs140914097;jsessionid=A7230B06A434D2CC66F33B0BD42BE921 (snp)


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      • Human Human A|C
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Type:
SNP
Organism:
Homo sapiens
Alleles:
A|C
Chromosomal Location:
chr 16 : 3426483 (build 36.3)
Strand:
+
Update Date:
Nov 14 2011
Associated Gene(s):
ZNF597
Related URLs:
NCBI dbSNP


ZNF597   (exon)  QuickView

Transcript CDS Change Protein Mutation Class AA Change
NM_152457
T1217G NP_689670 Missense F406C