Product Details

SNP ID
rs141499993
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.4:127730548 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CGGTTTTTATATCCTTCTCCATCAT[G/T]CATCGTGAGCCTGCGAAAAAGAAGG
Phenotype
MIM: 610796
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
SLC25A31 PubMed Links

Gene Details

Gene
SLC25A31
Gene Name
solute carrier family 25 member 31
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001318467.1 171 Missense Mutation ATG,ATT M1I NP_001305396.1
NM_031291.3 171 Missense Mutation ATG,ATT M1I NP_112581.1
XM_011532298.1 171 Missense Mutation ATG,ATT M1I XP_011530600.1

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