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 |
View Full Product Details