Product Details

SNP ID

rs1496969

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.6:99273732 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TATATACACATTCTCTAATCAATTA[C/T]AGGCATCTGGGTGCTACGCCTAAAG

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	8945	UTR 3			NP_115900.1
XM_006715582.2	8945	UTR 3			XP_006715645.1
XM_011536188.2	8945	UTR 3			XP_011534490.1
XM_011536189.2	8945	Intron			XP_011534491.1

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