Product Details

SNP ID
rs61995897
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:39383735 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CGGGCCTCATCTCCAATGATTCAGA[A/G]CTCACGTCCGTCGCTGCTGCAACCC
Phenotype
MIM: 610819
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
SLC25A38 PubMed Links

Gene Details

Gene
SLC25A38
Gene Name
solute carrier family 25 member 38
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_017875.2 411 Missense Mutation AAC,AGC N4S NP_060345.2
XM_006713214.1 411 UTR 5 XP_006713277.1
XM_011533869.2 411 Intron XP_011532171.1
XM_017006710.1 411 Missense Mutation AAC,AGC N4S XP_016862199.1

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