Product Details

SNP ID
rs6564313
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.16:76281057 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CTCACTGTGTTCTTTCTTTTCTCTG[A/G]TGGAAATAAAGGCCGTATCTGATAC
Phenotype
MIM: 610518
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
CNTNAP4 PubMed Links

Gene Details

Gene
CNTNAP4
Gene Name
contactin associated protein like 4
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001322178.1 Intron NP_001309107.1
NM_001322179.1 Intron NP_001309108.1
NM_001322180.1 Intron NP_001309109.1
NM_001322181.1 Intron NP_001309110.1
NM_001322187.1 Intron NP_001309116.1
NM_001322188.1 Intron NP_001309117.1
NM_001322189.1 Intron NP_001309118.1
NM_001322190.1 Intron NP_001309119.1
NM_001322191.1 Intron NP_001309120.1
NM_033401.4 Intron NP_207837.2
NM_138994.4 Intron NP_620481.2
XM_011523403.2 Intron XP_011521705.1
XM_017023805.1 Intron XP_016879294.1

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