Product Details

SNP ID
rs12269999
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:99027199 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TTAAGTGATTTTATTCCATGGCATA[C/T]ATGTAAGGGAACATCCATTTGCCCT
Phenotype
MIM: 607219
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
CNTN5 PubMed Links

Gene Details

Gene
CNTN5
Gene Name
contactin 5
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001243270.1 Intron NP_001230199.1
NM_001243271.1 Intron NP_001230200.1
NM_014361.3 Intron NP_055176.1
NM_175566.2 Intron NP_780775.1
XM_011542871.1 Intron XP_011541173.1
XM_011542873.1 Intron XP_011541175.1
XM_017017926.1 Intron XP_016873415.1
XM_017017927.1 Intron XP_016873416.1
XM_017017928.1 Intron XP_016873417.1
XM_017017929.1 Intron XP_016873418.1

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