Product Details

SNP ID
rs139743509
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.22:42168726 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTTCTGCAAGGGGGGGAGAGGGCAC[A/G]GAAGGGGAGGCTGACACGGGCAAAA
Phenotype
MIM: 603107
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
TCF20 PubMed Links

Gene Details

Gene
TCF20
Gene Name
transcription factor 20
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_005650.3 6131 Missense Mutation NP_005641.1
NM_181492.2 6131 Intron NP_852469.1
XM_005261722.3 6131 Missense Mutation XP_005261779.1
XM_006724313.3 6131 Missense Mutation XP_006724376.1
XM_011530353.2 6131 Intron XP_011528655.1
XM_011530354.2 6131 Intron XP_011528656.1

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