Product Details

SNP ID
rs151121275
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.4:52874055 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGCTTCAGGAGTCGTGTGGACAGCA[C/T]GATTACCTAACAACAGGAGAGGGCA
Phenotype
MIM: 612404
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
RASL11B PubMed Links

Gene Details

Gene
RASL11B
Gene Name
RAS like family 11 member B
There are no transcripts associated with this gene.

Gene
SCFD2
Gene Name
sec1 family domain containing 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_152540.3 2103 Missense Mutation ATG,GTG M657V NP_689753.2
XM_011534375.2 2103 Intron XP_011532677.1
XM_011534376.2 2103 Intron XP_011532678.1
XM_011534378.2 2103 Intron XP_011532680.1
XM_017007786.1 2103 Intron XP_016863275.1
XM_017007787.1 2103 Intron XP_016863276.1

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