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QuickView for rs116617903;jsessionid=280B897C586290C655C51E366B45D56C (snp)


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Type:
SNP
Organism:
Homo sapiens
Alleles:
T|C
Chromosomal Location:
chr 11 : 117933673 (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
A188G NP_064538 Missense K63R