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QuickView for rs1169313;jsessionid=5C2686B4649FB461834C8CBB6AD0509A (snp)


    • Macaque Macaque C
      • Human Human C|T
      • Chimp Chimp C
    • Mouse Mouse T
    • Rat Rat C
Type:
snp
Organism:
Homo sapiens
Alleles:
C|T
Chromosomal Location:
chr 12 : 119927053 (build 36.3)
Strand:
+
Flanking Sequence:
CTGAGCTCA [ C | T ] GATTTCTCCAG
Update Date:
May 25 2008
Validated:
YES
Associated Gene(s):
C12orf43HNF1A
Related URLs:
NCBI dbSNP


C12orf43   (intron)  QuickView

Transcript CDS Change Protein Mutation Class AA Change
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HNF1A   (intergenic)  QuickView

Transcript CDS Change Protein Mutation Class AA Change
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- - - -