Product Details

SNP ID: rs2699226
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.7:54759137 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TGTGGCCGCCCCGTTCGCCCGTACC[C/G]ACCGGTGGGAAGAAACTCACCTACC
Phenotype: MIM: 609215
Polymorphism: C/G, Transversion substitution
Allele Nomenclature
Literature Links: LOC100996654 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_001012456.1		Intron			NP_001012474.1
NM_014302.3		Intron			NP_055117.1