Product Details

SNP ID
rs13476983
Assay Type
Pre Designed
NCBI dbSNP Submissions
NA
Location
Chr.3:13776875 on Build GRCm38
Set Membership
Context Sequence [VIC/FAM]
GACGGGCAAAACACAAACAAGCAAC[A/G]TTACCAATAAGAATGACCCCAAGTC
Phenotype
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
Ralyl PubMed Links

Gene Details

Gene
Ralyl
Gene Name
RALY RNA binding protein-like
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001163328.1 433 Missense Mutation NP_001156800.1
NM_001163329.1 433 Intron NP_001156801.1
NM_001163330.1 433 Intron NP_001156802.1
NM_178631.4 433 Missense Mutation NP_848746.1

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