Product Details

SNP ID
rs2729046
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:2099727 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TCCAGCAACTTCTGGGGGGTTTCCA[A/G]TTTCTTTCGAGAGGCAAGACAACCG
Phenotype
MIM: 607280
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
CNTN4 PubMed Links

Gene Details

Gene
CNTN4
Gene Name
contactin 4
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001206955.1 48 Intron NP_001193884.1
NM_001206956.1 48 Intron NP_001193885.1
NM_175607.2 48 Intron NP_783200.1
NM_175613.2 48 Intron NP_783302.1
XM_006713004.3 48 Intron XP_006713067.1
XM_011533425.2 48 Intron XP_011531727.1
XM_011533426.2 48 Intron XP_011531728.1
XM_011533427.2 48 Intron XP_011531729.1
XM_011533428.2 48 Intron XP_011531730.1
XM_011533429.2 48 Intron XP_011531731.1
XM_011533430.2 48 Intron XP_011531732.1
XM_011533431.2 48 Intron XP_011531733.1
XM_017005782.1 48 Intron XP_016861271.1
XM_017005783.1 48 UTR 5 XP_016861272.1
XM_017005784.1 48 UTR 5 XP_016861273.1
XM_017005785.1 48 Intron XP_016861274.1
XM_017005786.1 48 Intron XP_016861275.1
XM_017005787.1 48 Intron XP_016861276.1
XM_017005788.1 48 Intron XP_016861277.1

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