Product Details

SNP ID
rs1010977
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:130345348 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGCTTATGATGATGGTTATTTTTGG[C/T]GAAAGCTAGGTAAAAAATAAGAAGC
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 Intron NP_001269124.1
NM_001282196.1 Intron NP_001269125.1
NM_001282197.1 Intron NP_001269126.1
NM_001282198.1 Intron NP_001269127.1
XM_005262489.4 Intron XP_005262546.1
XM_011531402.2 Intron XP_011529704.1
XM_011531403.1 Intron XP_011529705.1
XM_017029936.1 Intron XP_016885425.1
XM_017029937.1 Intron XP_016885426.1
XM_017029938.1 Intron XP_016885427.1
XM_017029939.1 Intron XP_016885428.1
XM_017029940.1 Intron XP_016885429.1
XM_017029941.1 Intron XP_016885430.1
XM_017029942.1 Intron XP_016885431.1
XM_017029943.1 Intron XP_016885432.1

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