Product Details

SNP ID: rs149278091
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.7:83366239 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TCTCCTGTGTAATCCACTTGCTTTC[A/G]ATTTTTATTTAGGTGAAAACATCTT
Phenotype: MIM: 608166
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: SEMA3E PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001178129.1	3660	UTR 3			NP_001171600.1
NM_012431.2	3660	UTR 3			NP_036563.1