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QuickView for rs113363630;jsessionid=978BC79641F8108384AE2868E41BD9A9 (snp)


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      • Human Human T|C
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Type:
SNP
Organism:
Homo sapiens
Alleles:
T|C
Chromosomal Location:
chr 22 : 44697233 (build 36.3)
Strand:
+
Update Date:
Nov 14 2011
Associated Gene(s):
WNT7B
Related URLs:
NCBI dbSNP


WNT7B   (UTR)  QuickView

Transcript CDS Change Protein Mutation Class AA Change
NM_058238
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