Product Details

SNP ID
rs144511019
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:143266888 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCTGGTAATTTATGGCTAGTTCATC[A/C]TGGTTTACAATGCATTCCACATCAT
Phenotype
MIM: 608396
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
SLC9A9 PubMed Links

Gene Details

Gene
SLC9A9
Gene Name
solute carrier family 9 member A9
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_173653.3 1961 Missense Mutation CAG,CAT Q584H NP_775924.1
XM_011512703.2 1961 Missense Mutation CAG,CAT Q368H XP_011511005.1
XM_011512704.2 1961 Intron XP_011511006.1
XM_017006202.1 1961 Intron XP_016861691.1
XM_017006203.1 1961 Missense Mutation CAG,CAT Q467H XP_016861692.1

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