Product Details

SNP ID
rs150594573
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.4:52865464 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ACTCATCAGCCAGCTCCACCAGCAC[A/G]TGCAGCAGCTACACCTGGGCACCCG
Phenotype
MIM: 612404
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
RASL11B PubMed Links

Gene Details

Gene
RASL11B
Gene Name
RAS like family 11 member B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_023940.2 586 Missense Mutation ATG,GTG M136V NP_076429.1
Gene
SCFD2
Gene Name
sec1 family domain containing 2
There are no transcripts associated with this gene.

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