Product Details

SNP ID
rs144930504
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.19:47432399 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGTGCATCACGTAGTCAAAGCACGA[C/T]GGCAGCCGCTCCTCCCGGGACCCGT
Phenotype
MIM: 601901
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
SLC8A2 PubMed Links

Gene Details

Gene
SLC8A2
Gene Name
solute carrier family 8 member A2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_015063.2 2226 Silent Mutation CCA,CCG P719P NP_055878.1
XM_005259172.1 2226 Silent Mutation CCA,CCG P713P XP_005259229.1
XM_017027159.1 2226 Silent Mutation CCA,CCG P143P XP_016882648.1

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