Product Details

SNP ID: rs2296896
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.13:112376360 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: ATGGGAAACTGTCAACCTTCAGAAC[A/G]TCCTTCTCCCTCAGCTGGAGGGAGC
Phenotype
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: SPACA7 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_145248.4	19	UTR 5			NP_660291.2
XM_011537466.1	19	Missense Mutation	CAT,CGT	H9R	XP_011535768.1
XM_011537467.2	19	Missense Mutation	CAT,CGT	H9R	XP_011535769.1
XM_011537468.2	19	UTR 5			XP_011535770.1
XM_011537471.2	19	UTR 5			XP_011535773.1
XM_011537472.2	19	Missense Mutation	CAT,CGT	H9R	XP_011535774.1
XM_017020391.1	19	Missense Mutation	CAT,CGT	H9R	XP_016875880.1
XM_017020392.1	19	UTR 5			XP_016875881.1