Product Details

SNP ID: rs11668026
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.19:17441824 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: ATGTCCCACATGTGAAAGCAAGGCC[A/C]AGGACTTTTTTTTTTTTTTTGGCTG
Phenotype
Polymorphism: A/C, Transversion substitution
Allele Nomenclature
Literature Links: TMEM221 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001190844.1		Intron			NP_001177773.1
XM_011527603.2		Intron			XP_011525905.1