Product Details

SNP ID: rs17129605
Assay Type: Functionally tested
NCBI dbSNP Submissions: 36
Location: Chr.1:86863628 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: ATACTACAAAAAAGAGGGACGTCAT[C/T]ATTACTTTCTGTTCAGAAACAACCT
Phenotype: MIM: 606254
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: SEP15 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_004261.3		Intron			NP_004252.2
NM_203341.1		Intron			NP_976086.1