Product Details

SNP ID
rs146921129
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:66366495 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTGGGGCTCATCTGGCTCTGATTCC[A/G]GCTCCTTCTCCAGGTCAAGATCCAG
Phenotype
MIM: 602110
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
LOC102724064 PubMed Links

Gene Details

Gene
LOC102724064
Gene Name
uncharacterized LOC102724064
There are no transcripts associated with this gene.

Gene
SLC29A2
Gene Name
solute carrier family 29 member 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001300868.1 1183 Missense Mutation NP_001287797.1
NM_001300869.1 1183 Intron NP_001287798.1
NM_001532.2 1183 Missense Mutation NP_001523.2
XM_011544974.1 1183 Missense Mutation XP_011543276.1
XM_017017630.1 1183 Missense Mutation XP_016873119.1
XM_017017631.1 1183 Missense Mutation XP_016873120.1
XM_017017632.1 1183 Missense Mutation XP_016873121.1
XM_017017633.1 1183 Missense Mutation XP_016873122.1
XM_017017634.1 1183 Intron XP_016873123.1
XM_017017635.1 1183 Intron XP_016873124.1
XM_017017636.1 1183 Missense Mutation XP_016873125.1
XM_017017637.1 1183 Intron XP_016873126.1
XM_017017638.1 1183 Missense Mutation XP_016873127.1

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