Product Details

SNP ID
rs149867707
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:66133829 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTCGAGTGGAGCCCTGATGAAGTTC[A/G]TGCTCATGGTTGCCCAGCCATTAAC
Phenotype
MIM: 611037
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
SLC25A26 PubMed Links

Gene Details

Gene
SLC25A26
Gene Name
solute carrier family 25 member 26
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001164796.1 220 Intron NP_001158268.1
NM_173471.3 220 UTR 5 NP_775742.4
XM_006712956.1 220 Intron XP_006713019.1
XM_011533327.2 220 Intron XP_011531629.1
XM_011533328.1 220 Intron XP_011531630.1
XM_017005671.1 220 Intron XP_016861160.1
XM_017005672.1 220 Intron XP_016861161.1
XM_017005673.1 220 Intron XP_016861162.1
XM_017005674.1 220 Intron XP_016861163.1

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