Product Details

SNP ID
rs2946676
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.15:65051697 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
AAATCTAGAGAGGGGTCACTTAGGG[A/G]TCATTGCTGTCCACCCTTTGGGACA
Phenotype
MIM: 612085
Polymorphism
A/G, 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_001307930.1 881 Intron NP_001294859.1
NM_016563.3 881 Intron NP_057647.1
XM_005254434.4 881 Intron XP_005254491.1
XM_011521660.2 881 Intron XP_011519962.1
XM_017022296.1 881 UTR 3 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_178859.3 881 Intron NP_849190.2
XM_005254159.4 881 Intron XP_005254216.1

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