Product Details

SNP ID
rs149875382
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:103590914 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTACACAGGCAAGAAGATGTGATAG[G/T]AAGTCTCTTCTTACAATTAGGACCG
Phenotype
MIM: 608561
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
STAB2 PubMed Links

Gene Details

Gene
STAB2
Gene Name
stabilin 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_017564.9 326 Missense Mutation AGG,AGT R33S NP_060034.9
XM_011538537.2 326 Missense Mutation AGG,AGT R33S XP_011536839.1
XM_011538538.2 326 Missense Mutation AGG,AGT R33S XP_011536840.1
XM_011538539.2 326 Intron XP_011536841.1
XM_011538541.2 326 Intron XP_011536843.1
XM_011538542.2 326 Intron XP_011536844.1
XM_017019585.1 326 Missense Mutation AGG,AGT R33S XP_016875074.1

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