Product Details

SNP ID
rs146669253
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:135242820 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TAAGGCAAAGAGTCATATTCCAGAA[C/T]TGGAGCAAACCCTGGATAATTTGCT
Phenotype
MIM: 609987
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
STRA8 PubMed Links

Gene Details

Gene
STRA8
Gene Name
stimulated by retinoic acid 8
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_182489.1 938 Silent Mutation CTG,TTG L100L NP_872295.1
XM_011516137.2 938 Silent Mutation CTG,TTG L78L XP_011514439.1
XM_011516138.2 938 Silent Mutation CTG,TTG L78L XP_011514440.1
XM_011516139.2 938 Silent Mutation CTG,TTG L78L XP_011514441.1
XM_017012150.1 938 Silent Mutation CTG,TTG L78L XP_016867639.1

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