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QuickView for rs146150499;jsessionid=624B650E1B6846466BB640E5FE55248A (snp)


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Type:
SNP
Organism:
Homo sapiens
Alleles:
T|C
Chromosomal Location:
chr 8 : 91062228 (build 36.3)
Strand:
+
Update Date:
Nov 14 2011
Associated Gene(s):
NBN
Related URLs:
NCBI dbSNP


NBN   (exon)  QuickView

Transcript CDS Change Protein Mutation Class AA Change
NM_001024688
A144G NP_001019859 Synonymous Q48Q
NM_002485
A390G NP_002476 Synonymous Q130Q