Product Details

SNP ID
rs142436732
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.15:65053106 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AACTTGGCCCAGGTGGAACTTGAGT[C/T]AAAAGAGAGAGATGTGCTGTCAGTT
Phenotype
MIM: 612085
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
RASL12 PubMed Links

Gene Details

Gene
RASL12
Gene Name
RAS like family 12
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001307930.1 625 Intron NP_001294859.1
NM_016563.3 625 Intron NP_057647.1
XM_005254434.4 625 Intron XP_005254491.1
XM_011521660.2 625 Intron XP_011519962.1
XM_017022296.1 625 Intron XP_016877785.1
Gene
SLC51B
Gene Name
solute carrier family 51 beta subunit
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_178859.3 625 Missense Mutation TCA,TTA S110L NP_849190.2
XM_005254159.4 625 Missense Mutation TCA,TTA S110L XP_005254216.1

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