Correlation Engine 2.0
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QuickView for rs138200523;jsessionid=543B2CA62A4142C93CC1A89E77710483 (snp)


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      • Human Human A|C
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Type:
SNP
Organism:
Homo sapiens
Alleles:
A|C
Chromosomal Location:
chr 17 : 71986494 (build 36.3)
Strand:
+
Update Date:
Nov 14 2011
Associated Gene(s):
RHBDF2
Related URLs:
NCBI dbSNP


RHBDF2   (exon)  QuickView

Transcript CDS Change Protein Mutation Class AA Change
NM_001005498
G661T NP_001005498 Missense A221S
NM_024599
G748T NP_078875 Missense A250S