Product Details

SNP ID
rs142082056
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:74592121 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTAACATGGTCTGAATTGCAACAGA[C/T]GTAGTCTCACTTAAACCAGTATTTA
Phenotype
MIM: 300379
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
RLIM PubMed Links

Gene Details

Gene
RLIM
Gene Name
ring finger protein, LIM domain interacting
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_016120.3 1484 Silent Mutation ACA,ACG T398T NP_057204.2
NM_183353.2 1484 Silent Mutation ACA,ACG T398T NP_899196.1

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