Product Details

SNP ID
rs139107749
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.10:68483542 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GATAAACCACGATAGAGTCCTTTTC[A/G]AATTCCATGGTGTCCATAGACATAC
Phenotype
MIM: 139080
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
SLC25A16 PubMed Links

Gene Details

Gene
SLC25A16
Gene Name
solute carrier family 25 member 16
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001324312.1 1037 Missense Mutation NP_001311241.1
NM_001324313.1 1037 Intron NP_001311242.1
NM_001324314.1 1037 Missense Mutation NP_001311243.1
NM_001324315.1 1037 Missense Mutation NP_001311244.1
NM_001324317.1 1037 Missense Mutation NP_001311246.1
NM_152707.3 1037 Missense Mutation NP_689920.1
XM_011540211.2 1037 Nonsense Mutation XP_011538513.1
XM_017016695.1 1037 Intron XP_016872184.1

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