Correlation Engine 2.0
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QuickView for rs150643626;jsessionid=280B897C586290C655C51E366B45D56C (snp)


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      • Human Human C|G
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Type:
SNP
Organism:
Homo sapiens
Alleles:
C|G
Chromosomal Location:
chr 11 : 117932968 (build 36.3)
Strand:
+
Update Date:
Nov 14 2011
Associated Gene(s):
IFT46
Related URLs:
NCBI dbSNP


IFT46   (exon)  QuickView

Transcript CDS Change Protein Mutation Class AA Change
NM_020153
G201C NP_064538 Missense E67D