Product Details

SNP ID
rs183860204
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.10:68483456 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTTAGTTGAGGTGAAAAAACTGCTT[C/T]ATAAGTTCGTATGTTGTAAAAGCCA
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 1123 UTR 3 NP_001311241.1
NM_001324313.1 1123 Intron NP_001311242.1
NM_001324314.1 1123 Missense Mutation ATA,ATG I227M NP_001311243.1
NM_001324315.1 1123 Missense Mutation ATA,ATG I227M NP_001311244.1
NM_001324317.1 1123 Missense Mutation ATA,ATG I191M NP_001311246.1
NM_152707.3 1123 Missense Mutation ATA,ATG I325M NP_689920.1
XM_011540211.2 1123 Missense Mutation ATA,ATG I325M XP_011538513.1
XM_017016695.1 1123 Intron XP_016872184.1

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