Product Details

SNP ID

rs9389187

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.6:99275065 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTAGAAGCCATGGGGTAACTAAAAA[C/T]AAAAAAGGTATTAAATAAGGAAAAA

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	7612	UTR 3			NP_115900.1
XM_006715582.2	7612	UTR 3			XP_006715645.1
XM_011536188.2	7612	UTR 3			XP_011534490.1
XM_011536189.2	7612	Intron			XP_011534491.1

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