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QuickView for rs143019903;jsessionid=BF83EDCDFC5ED1CFA79410C15FD20F59 (snp)


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Type:
SNP
Organism:
Homo sapiens
Alleles:
A|T
Chromosomal Location:
chr 7 : 114058896 (build 36.3)
Strand:
+
Update Date:
Nov 14 2011
Associated Gene(s):
FOXP2
Related URLs:
NCBI dbSNP


FOXP2   (exon)  QuickView

Transcript CDS Change Protein Mutation Class AA Change
NM_014491
A675T NP_055306 Missense Q225H
NM_148898
A750T NP_683696 Missense Q250H
NM_148899
A399T NP_683697 Missense Q133H