Product Details

SNP ID: rs1462855
Assay Type: Functionally tested
NCBI dbSNP Submissions: 67
Location: Chr.1:155081243 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: AGTACTTCCATTTAGTCCCGTGGAA[C/T]AGGAGAGACCTGTTCCCAATCTGGC
Phenotype: MIM: 601381
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: EFNA3 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_004952.4		Intron			NP_004943.1