Correlation Engine 2.0
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QuickView for rs149037850;jsessionid=4632FE608AB397A69FEFEB512701098A (snp)


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      • Human Human A|G
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Type:
SNP
Organism:
Homo sapiens
Alleles:
A|G
Chromosomal Location:
chr 2 : 173538636 (build 36.3)
Strand:
+
Update Date:
Nov 14 2011
Associated Gene(s):
RAPGEF4
Related URLs:
NCBI dbSNP


RAPGEF4   (exon)  QuickView

Transcript CDS Change Protein Mutation Class AA Change
NM_001100397
G367A NP_001093867 Missense E123K
NM_007023
G799A NP_008954 Missense E267K