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QuickView for rs78513281;jsessionid=F10B03D6372FEADEAD78D062DCD3663D (snp)


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      • Human Human A|C
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Type:
SNP
Organism:
Homo sapiens
Alleles:
A|C
Chromosomal Location:
chr 15 : 77011841 (build 36.3)
Strand:
+
Update Date:
Nov 14 2011
Associated Gene(s):
CTSH
Related URLs:
NCBI dbSNP


CTSH   (exon)  QuickView

Transcript CDS Change Protein Mutation Class AA Change
NM_004390
T420G NP_004381 Missense S140R
NM_148979
T384G NP_683880 Missense S128R