Product Details

SNP ID
rs1136645
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.10:68482756 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TTTCATGATGTTGCATAGGCTGGCA[C/T]GGAATTCCAGGGCTCAAGTGATCCT
Phenotype
MIM: 139080
Polymorphism
C/T, 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 2680 UTR 3 NP_001311241.1
NM_001324313.1 2680 Intron NP_001311242.1
NM_001324314.1 2680 UTR 3 NP_001311243.1
NM_001324315.1 2680 UTR 3 NP_001311244.1
NM_001324317.1 2680 UTR 3 NP_001311246.1
NM_152707.3 2680 UTR 3 NP_689920.1
XM_011540211.2 2680 Intron XP_011538513.1
XM_017016695.1 2680 Intron XP_016872184.1

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