Product Details

SNP ID
rs201390440
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:102718427 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TATGTTGTCCAAATCCATCTACTCA[C/T]TTTTTAATTTACTATTCCCATCACC
Phenotype
MIM: 600530
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
MFSD9 PubMed Links

Gene Details

Gene
MFSD9
Gene Name
major facilitator superfamily domain containing 9
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001322080.1 1436 Missense Mutation AAT,AGT N412S NP_001309009.1
NM_001322081.1 1436 Missense Mutation AAT,AGT N412S NP_001309010.1
NM_032718.4 1436 Missense Mutation AAT,AGT N473S NP_116107.3
XM_011512005.2 1436 Missense Mutation AAT,AGT N412S XP_011510307.1
XM_011512006.2 1436 Missense Mutation AAT,AGT N348S XP_011510308.1
XM_011512007.2 1436 Missense Mutation AAT,AGT N332S XP_011510309.1
Gene
SLC9A2
Gene Name
solute carrier family 9 member A2
There are no transcripts associated with this gene.

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