Product Details

SNP ID
rs139787750
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.14:100290080 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCAGAGGGCAGGCAGCCGCAGGGTT[C/T]GTGGAGAAGCCCCAGGGTGAGCAGG
Phenotype
MIM: 615064
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
SLC25A29 PubMed Links

Gene Details

Gene
SLC25A29
Gene Name
solute carrier family 25 member 29
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001039355.2 Intron NP_001034444.1
NM_001291813.1 Intron NP_001278742.1
NM_001291814.1 Intron NP_001278743.1
NM_152333.3 Intron NP_689546.1
XM_006720038.1 Intron XP_006720101.1
XM_006720039.3 Intron XP_006720102.1
XM_011536443.1 Intron XP_011534745.1
XM_011536444.1 Intron XP_011534746.1
XM_011536446.1 Intron XP_011534748.1
XM_011536447.1 Intron XP_011534749.1
XM_011536448.1 Intron XP_011534750.1
XM_011536449.2 Intron XP_011534751.1
XM_017020979.1 Intron XP_016876468.1
XM_017020980.1 Intron XP_016876469.1
XM_017020981.1 Intron XP_016876470.1
XM_017020982.1 Intron XP_016876471.1
XM_017020983.1 Intron XP_016876472.1
XM_017020984.1 Intron XP_016876473.1
XM_017020985.1 Intron XP_016876474.1
XM_017020986.1 Intron XP_016876475.1
XM_017020987.1 Intron XP_016876476.1
XM_017020988.1 Intron XP_016876477.1

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