Product Details

SNP ID
rs76398659
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.8:23533590 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTTTTAGTCTTGGGCTTCTGACTCT[C/T]TCTGACTTCAGGGGTTTCCTTCTTC
Phenotype
MIM: 610387
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
SLC25A37 PubMed Links

Gene Details

Gene
SLC25A37
Gene Name
solute carrier family 25 member 37
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001317812.1 Intron NP_001304741.1
NM_001317813.1 Intron NP_001304742.1
NM_001317814.1 Intron NP_001304743.1
NM_016612.3 Intron NP_057696.2
XM_006716352.3 Intron XP_006716415.1
XM_011544550.2 Intron XP_011542852.1
XM_011544553.2 Intron XP_011542855.1
XM_011544554.2 Intron XP_011542856.1
XM_017013532.1 Intron XP_016869021.1

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