Product Details

SNP ID
rs190633524
Assay Type
Functionally tested
NCBI dbSNP Submissions
1
Location
Chr.1:168281100 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGTTCGAGAAGTGCCTATGGCCATG[A/G]GTGAGCTGGGCACTCGGAAGCCCAG
Phenotype
MIM: 604614
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
TBX19 PubMed Links

Gene Details

Gene
TBX19
Gene Name
T-box 19
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_005149.2 61 Missense Mutation AGT,GGT S4G NP_005140.1

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