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QuickView for rs142551001;jsessionid=8C7BBEE13AD88865441EE0AFB582E8B7 (snp)


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      • Human Human A|G
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Type:
SNP
Organism:
Homo sapiens
Alleles:
A|G
Chromosomal Location:
chr 16 : 23290603 (build 36.3)
Strand:
+
Update Date:
Nov 14 2011
Associated Gene(s):
SCNN1B
Related URLs:
NCBI dbSNP


SCNN1B   (exon)  QuickView

Transcript CDS Change Protein Mutation Class AA Change
NM_000336
G1050A NP_000327 Synonymous K350K