Product Details

SNP ID: rs79834971
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.4:70601066 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CTCTCTCCGTTGACTGGGGGACAAA[G/T]ATTTATAACAAATAATTATCATCCA
Phenotype: MIM: 601259
Polymorphism: G/T, Transversion substitution
Allele Nomenclature
Literature Links: AMBN PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_016519.5		Intron			NP_057603.1