Product Details

SNP ID
rs185505099
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.X:70925889 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCTAGACTTGCGTGAGGGTTGGTTA[C/G]TCTTAATCTCTTCCAGGCTGTGCTG
Phenotype
MIM: 300443
Polymorphism
C/G, Transversion Substitution
Allele Nomenclature
Literature Links
SLC7A3 PubMed Links

Gene Details

Gene
SLC7A3
Gene Name
solute carrier family 7 member 3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001048164.2 1958 Missense Mutation ACT,AGT T595S NP_001041629.1
NM_032803.5 1958 Missense Mutation ACT,AGT T595S NP_116192.4
XM_017029912.1 1958 Missense Mutation ACT,AGT T595S XP_016885401.1

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