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QuickView for rs149786664;jsessionid=770780A795AED8DF99572C401482E993 (snp)


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      • Human Human C|G
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    • Mouse Mouse -
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Type:
SNP
Organism:
Homo sapiens
Alleles:
C|G
Chromosomal Location:
chr 8 : 11740066 (build 36.3)
Strand:
+
Update Date:
Nov 14 2011
Associated Gene(s):
CTSB
Related URLs:
NCBI dbSNP


CTSB   (exon)  QuickView

Transcript CDS Change Protein Mutation Class AA Change
NM_001908
G997C NP_001899 Missense D333H
NM_147780
G997C NP_680090 Missense D333H
NM_147781
G997C NP_680091 Missense D333H
NM_147782
G997C NP_680092 Missense D333H
NM_147783
G997C NP_680093 Missense D333H