Product Details

SNP ID
rs144881079
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:74266614 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTGAAGTTTTATTTGTGTTCAGTAC[G/T]TGTACGTTATTTTGACTGCTAGTCC
Phenotype
MIM: 601325
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
CNTN3 PubMed Links

Gene Details

Gene
CNTN3
Gene Name
contactin 3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_020872.2 1560 Missense Mutation CAA,CAC Q951H NP_065923.1
XM_005264757.3 1560 Missense Mutation CAA,CAC Q951H XP_005264814.1
XM_011533768.2 1560 Missense Mutation CAA,CAC Q951H XP_011532070.1
XM_017006507.1 1560 Missense Mutation CAA,CAC Q951H XP_016861996.1
XM_017006508.1 1560 Missense Mutation CAA,CAC Q893H XP_016861997.1
XM_017006509.1 1560 Missense Mutation CAA,CAC Q509H XP_016861998.1

View Full Product Details