Product Details

SNP ID: rs2235308
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.X:129651235 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: CAGCCGGGCCCTGGAGAGCAGCCCC[A/G]GGCTTCTTGCATCCCTCCCATTGCG
Phenotype: MIM: 300297
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: APLN PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_017413.4		Intron			NP_059109.3