Product Details

SNP ID
rs144779737
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.3:143266832 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGCTTTCTGGTCCAGACCTAGCCTT[G/T]CAGGAGGACTGCAGGGTGAGGAGGC
Phenotype
MIM: 608396
Polymorphism
G/T, 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 2017 Missense Mutation GAA,GCA E603A NP_775924.1
XM_011512703.2 2017 Missense Mutation GAA,GCA E387A XP_011511005.1
XM_011512704.2 2017 Intron XP_011511006.1
XM_017006202.1 2017 Intron XP_016861691.1
XM_017006203.1 2017 Missense Mutation GAA,GCA E486A XP_016861692.1

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