Correlation Engine 2.0
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QuickView for rs111381779;jsessionid=0670E97E27C601C48E45BA1FFCC07530 (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 : 65444953 (build 36.3)
Strand:
+
Update Date:
Nov 14 2011
Associated Gene(s):
C11orf68DRAP1
Related URLs:
NCBI dbSNP


C11orf68   (intergenic)  QuickView

Transcript CDS Change Protein Mutation Class AA Change
-
- - - -

DRAP1   (exon)  QuickView

Transcript CDS Change Protein Mutation Class AA Change
NM_006442
C446G NP_006433 Missense T149S