Product Details

SNP ID
rs138592266
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.10:102469149 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCTTCCTGCTCTACTATGTGGACAC[C/T]TTTGTCTCAGTGTACAAGATCAACA
Phenotype
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
MFSD13A PubMed Links

Gene Details

Gene
MFSD13A
Gene Name
major facilitator superfamily domain containing 13A
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_024789.3 962 Silent Mutation ACC,ACT T40T NP_079065.2
XM_006717973.3 962 Silent Mutation ACC,ACT T40T XP_006718036.1
XM_006717974.3 962 Silent Mutation ACC,ACT T40T XP_006718037.1
XM_011540160.2 962 Silent Mutation ACC,ACT T40T XP_011538462.1
XM_011540163.2 962 Silent Mutation ACC,ACT T40T XP_011538465.1
XM_011540167.2 962 Silent Mutation ACC,ACT T40T XP_011538469.1
XM_011540169.2 962 Silent Mutation ACC,ACT T40T XP_011538471.1
XM_017016654.1 962 Silent Mutation ACC,ACT T40T XP_016872143.1
XM_017016655.1 962 Silent Mutation ACC,ACT T40T XP_016872144.1
XM_017016656.1 962 Silent Mutation ACC,ACT T40T XP_016872145.1
XM_017016657.1 962 Silent Mutation ACC,ACT T40T XP_016872146.1
XM_017016658.1 962 Silent Mutation ACC,ACT T40T XP_016872147.1
XM_017016659.1 962 Silent Mutation ACC,ACT T40T XP_016872148.1
XM_017016660.1 962 Intron XP_016872149.1
XM_017016661.1 962 Silent Mutation ACC,ACT T40T XP_016872150.1
XM_017016662.1 962 Silent Mutation ACC,ACT T40T XP_016872151.1

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