Product Details

SNP ID
rs200502867
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.11:57488931 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ACAGACTCACACTGCAGCATAGAGA[C/T]TCCCACAGGCTGAGTGGAAGAAACC
Phenotype
MIM: 603733
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
SLC43A1 PubMed Links

Gene Details

Gene
SLC43A1
Gene Name
solute carrier family 43 member 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001198810.1 1489 Missense Mutation AAT,AGT N465S NP_001185739.1
NM_003627.5 1489 Missense Mutation AAT,AGT N465S NP_003618.1
XM_005274358.4 1489 Missense Mutation AAT,AGT N481S XP_005274415.1
XM_011545320.2 1489 Missense Mutation AAT,AGT N450S XP_011543622.1
XM_011545321.2 1489 Missense Mutation AAT,AGT N209S XP_011543623.1
XM_011545322.1 1489 Missense Mutation AAT,AGT N209S XP_011543624.1
XM_017018451.1 1489 Missense Mutation AAT,AGT N465S XP_016873940.1
XM_017018452.1 1489 Missense Mutation AAT,AGT N434S XP_016873941.1
XM_017018453.1 1489 Missense Mutation AAT,AGT N209S XP_016873942.1

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