Product Details

SNP ID
rs1804589
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.13:44434291 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGCGCAAGCAGGAGAGAGAACCCTT[A/G]GAAGTGAGGGGTAGGGAGCCGGAAG
Phenotype
MIM: 607715
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
TSC22D1 PubMed Links

Gene Details

Gene
TSC22D1
Gene Name
TSC22 domain family member 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001243797.1 729 UTR 3 NP_001230726.1
NM_001243798.1 729 UTR 3 NP_001230727.1
NM_001243799.1 729 Intron NP_001230728.1
NM_006022.3 729 UTR 3 NP_006013.1
NM_183422.3 729 UTR 3 NP_904358.2
XM_005266583.4 729 Intron XP_005266640.1
XM_017020810.1 729 Intron XP_016876299.1
XM_017020811.1 729 Intron XP_016876300.1

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