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SNP ID:
rs144264123
Gene
SLC29A4 TNRC18
Gene Name
Set Membership:
-
Chromosome Location:
Chr.7: 5297183 - 5297183 on Build GRCh38
Polymorphism:
C/G, Transversion substitution
Context Sequence [VIC/FAM]:

ACCGCGTGCACCACGACGTTGTCGC[C/G]GGGGACGTCCACTTCGTAAGTGCGC

Assay ID C_173118543_10
Size
Availability Made To Order
Catalog # 4351379
Price
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Assay Details



Species:

 Human

dbSNP Submissions:

 NA

Phenotype:

 MIM: 609149

Literature Links:

 SLC29A4 PubMed Links

Allele Nomenclature:

Minor Allele Frequency:
1000Genome Applied Biosystems® HapMap
Global - Not Available Caucasian - Not Available CEPH (CEU) - Not Available
EAS - Not Available African American - Not Available YRI (Yoruba) - Not Available
SAS - Not Available Chinese - Not Available CHB (Han Chinese) - Not Available
AFR - Not Available Japanese - Not Available JPT (Japanese) - Not Available
EUR - Not Available
AMR - Not Available
SLC29A4 - solute carrier family 29 member 4
Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid Protein ID
NM_001040661.1 1048 Silent Mutation GCC,GCG A,A 289 NP_001035751.1
NM_001300847.1 1048 Silent Mutation GCC,GCG A,A 275 NP_001287776.1
NM_153247.2 1048 Silent Mutation GCC,GCG A,A 289 NP_694979.2
XM_005249658.4 1048 Silent Mutation GCC,GCG A,A 275 XP_005249715.1
XM_006715667.3 1048 Silent Mutation GCC,GCG A,A 289 XP_006715730.1
XM_006715668.2 1048 Silent Mutation GCC,GCG A,A 97 XP_006715731.1
XM_011515200.2 1048 Silent Mutation GCC,GCG A,A 289 XP_011513502.1
XM_011515201.2 1048 Silent Mutation GCC,GCG A,A 289 XP_011513503.1
TNRC18 - trinucleotide repeat containing 18
There are no transcripts associated with this gene.

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