Product Details

SNP ID

rs79111430

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.6:99274057 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AAAACAAAATGTACATTACTTTGTA[C/T]AATTTTATATTTATAAAATGAAAAA

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	8620	UTR 3			NP_115900.1
XM_006715582.2	8620	UTR 3			XP_006715645.1
XM_011536188.2	8620	UTR 3			XP_011534490.1
XM_011536189.2	8620	Intron			XP_011534491.1

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