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QuickView for rs113780841;jsessionid=2F2635F612CAC0BD191DDF59C162B094 (snp)


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      • Human Human A|G
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Type:
SNP
Organism:
Homo sapiens
Alleles:
A|G
Chromosomal Location:
chr 12 : 2838299 (build 36.3)
Strand:
+
Update Date:
Nov 14 2011
Associated Gene(s):
FOXM1
Related URLs:
NCBI dbSNP


FOXM1   (exon)  QuickView

Transcript CDS Change Protein Mutation Class AA Change
NM_021953
C2058T NP_068772 Synonymous S686S
NM_202002
C2172T NP_973731 Synonymous S724S
NM_202003
C2013T NP_973732 Synonymous S671S