Product Details

SNP ID
rs145386095
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:130350719 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TATCTTCCACTATAGCCAATCCCAC[C/T]GATGTTCTAAAGGTAAGAGAGATAC
Phenotype
MIM: 300242
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
SLC25A14 PubMed Links

Gene Details

Gene
SLC25A14
Gene Name
solute carrier family 25 member 14
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001282195.1 766 Silent Mutation ACC,ACT T162T NP_001269124.1
NM_001282196.1 766 Silent Mutation ACC,ACT T159T NP_001269125.1
NM_001282197.1 766 Silent Mutation ACC,ACT T159T NP_001269126.1
NM_001282198.1 766 Silent Mutation ACC,ACT T127T NP_001269127.1
XM_005262489.4 766 Silent Mutation ACC,ACT T61T XP_005262546.1
XM_011531402.2 766 Silent Mutation ACC,ACT T171T XP_011529704.1
XM_011531403.1 766 Intron XP_011529705.1
XM_017029936.1 766 Silent Mutation ACC,ACT T127T XP_016885425.1
XM_017029937.1 766 Silent Mutation ACC,ACT T171T XP_016885426.1
XM_017029938.1 766 Silent Mutation ACC,ACT T162T XP_016885427.1
XM_017029939.1 766 Silent Mutation ACC,ACT T159T XP_016885428.1
XM_017029940.1 766 Silent Mutation ACC,ACT T61T XP_016885429.1
XM_017029941.1 766 Silent Mutation ACC,ACT T18T XP_016885430.1
XM_017029942.1 766 Silent Mutation ACC,ACT T18T XP_016885431.1
XM_017029943.1 766 Intron XP_016885432.1

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