Correlation Engine 2.0
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QuickView for rs144771892;jsessionid=770780A795AED8DF99572C401482E993 (snp)


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      • Human Human G|C
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    • Mouse Mouse -
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Type:
SNP
Organism:
Homo sapiens
Alleles:
G|C
Chromosomal Location:
chr 8 : 11745814 (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
C297G NP_001899 Missense I99M
NM_147780
C297G NP_680090 Missense I99M
NM_147781
C297G NP_680091 Missense I99M
NM_147782
C297G NP_680092 Missense I99M
NM_147783
C297G NP_680093 Missense I99M