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QuickView for rs146216998;jsessionid=5B08FF5661A85316E4B42C462E538440 (snp)


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      • Human Human A|C
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Type:
SNP
Organism:
Homo sapiens
Alleles:
A|C
Chromosomal Location:
chr 14 : 91321450 (build 36.3)
Strand:
+
Update Date:
Nov 14 2011
Associated Gene(s):
TC2N
Related URLs:
NCBI dbSNP


TC2N   (exon)  QuickView

Transcript CDS Change Protein Mutation Class AA Change
NM_152332
G1171T NP_689545 Missense V391L