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QuickView for rs77086875;jsessionid=859D6FAF200A54CE6304E1A311799B3C (snp)


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      • Human Human G|C
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Type:
SNP
Organism:
Homo sapiens
Alleles:
G|C
Chromosomal Location:
chr 11 : 64093788 (build 36.3)
Strand:
+
Update Date:
Nov 14 2011
Associated Gene(s):
SLC22A11
Related URLs:
NCBI dbSNP


SLC22A11   (exon)  QuickView

Transcript CDS Change Protein Mutation Class AA Change
NM_018484
C1471G NP_060954 Missense L491V