Product Details
- SNP ID
-
rs142143651
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.19:45872336 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GAAGGAGATGCCGAAGGGGTATCGG[C/T]GGCCCCTGGCACACGCCAAGCCACC
- Phenotype
-
MIM: 602295
MIM: 602388
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
FOXA3
PubMed Links
Gene Details
- Gene
- FOXA3
- Gene Name
- forkhead box A3
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_004497.2 |
528 |
Missense Mutation |
CGG,TGG |
R111W |
NP_004488.2 |
- Gene
- SYMPK
- Gene Name
- symplekin
There are no transcripts associated with this gene.
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