Product Details

SNP ID
rs1045731
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.6:99273127 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
AGATCCAGAAATAAACACTGAAATG[C/T]CATCTTCACATTGGGGTCATCATTC
Phenotype
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
FAXC PubMed Links

Gene Details

Gene
FAXC
Gene Name
failed axon connections homolog
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_032511.2 9550 UTR 3 NP_115900.1
XM_006715582.2 9550 UTR 3 XP_006715645.1
XM_011536188.2 9550 UTR 3 XP_011534490.1
XM_011536189.2 9550 Intron XP_011534491.1

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