Product Details

SNP ID
rs201392610
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.10:99613781 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTTCGTAGCAGGCAAAATAAAGGGC[A/G]TGGGCAGGCCCTGCGCCTGTTGCTG
Phenotype
MIM: 609767
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
SLC25A28 PubMed Links

Gene Details

Gene
SLC25A28
Gene Name
solute carrier family 25 member 28
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_031212.3 450 Silent Mutation CAC,CAT H145H NP_112489.3
XM_005270208.1 450 Silent Mutation CAC,CAT H46H XP_005270265.1
XM_005270211.4 450 Silent Mutation CAC,CAT H46H XP_005270268.1
XM_006718005.3 450 Silent Mutation CAC,CAT H46H XP_006718068.1
XM_006718006.3 450 Silent Mutation CAC,CAT H145H XP_006718069.1
XM_011540239.2 450 Silent Mutation CAC,CAT H55H XP_011538541.1
XM_011540240.1 450 Silent Mutation CAC,CAT H46H XP_011538542.1
XM_011540244.2 450 Silent Mutation CAC,CAT H145H XP_011538546.1
XM_017016741.1 450 Silent Mutation CAC,CAT H46H XP_016872230.1
XM_017016742.1 450 UTR 5 XP_016872231.1

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