Product Details

SNP ID: rs219294
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.14:60092943 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: CTCTGTATCCATCATTTTTCACTTA[C/T]TCATTTTTTACTATTTTTAGGTGTT
Phenotype
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: PCNX4 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_022495.5		Intron			NP_071940.4
XM_005268009.2		Intron			XP_005268066.1