Product Details
- SNP ID
-
rs4447177
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.11:22624479 on Build GRCh38
- Set Membership
-
HapMap
- Context Sequence [VIC/FAM]
- TGCTAATTCCATGGCTTTAAGTGGA[A/G]TACTTCCAATCACTTCCTCTATCCA
- Phenotype
-
MIM: 613897
MIM: 602835
- Polymorphism
- A/G, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
FANCF
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs45473997] are located under a primer sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.
Gene Details
- Gene
- FANCF
- Gene Name
- Fanconi anemia complementation group F
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_022725.3 |
1363 |
UTR 3 |
|
|
NP_073562.1 |
- Gene
- GAS2
- Gene Name
- growth arrest specific 2
There are no transcripts associated with this gene.
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