Product Details

SNP ID
rs146545642
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:113817614 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGGACGAAACAGGCAGACCTCCGGG[C/T]CTGGCTTGGGATCCCAGTGGCACCC
Phenotype
MIM: 616444
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
RBM19 PubMed Links

Gene Details

Gene
RBM19
Gene Name
RNA binding motif protein 19
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001146698.1 3543 Intron NP_001140170.1
NM_001146699.1 3543 UTR 3 NP_001140171.1
NM_016196.3 3543 Intron NP_057280.2
XM_017020280.1 3543 UTR 3 XP_016875769.1
XM_017020281.1 3543 Intron XP_016875770.1

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