Product Details

SNP ID: rs17076886
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.13:19181472 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: TCAGGAGGCGGCACCACTGTTTGCT[C/T]TCTGGGGGACAGGACACGGTCAATG
Phenotype: MIM: 602528
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: LOC101928697 PubMed Links

Gene Details

There are no transcripts associated with this gene.

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_006001.2		Intron			NP_005992.1