Product Details

SNP ID: rs6710785
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.2:238166000 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: TCATCCTGAGGCCCAGTACTCCTGG[A/C]CACCACAAGCCCGCTGAAGGGACTG
Phenotype: MIM: 615099
Polymorphism: A/C, Transversion substitution
Allele Nomenclature
Literature Links: ERFE PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001291832.1		Intron			NP_001278761.1

There are no transcripts associated with this gene.