Product Details
- SNP ID
-
rs4652762
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
43
- Location
-
Chr.1:183024825 on Build GRCh38
- Set Membership
-
HapMap
- Context Sequence [VIC/FAM]
- TGTCCCTGGGTAAAAAGGCTCTCCT[C/T]TACTGTCTTCCCTTTTGCTTTCATT
- Phenotype
-
MIM: 150290
- Polymorphism
- C/T, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
LAMC1
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs77619662] are located under a probe 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
- LAMC1
- Gene Name
- laminin subunit gamma 1
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_002293.3 |
|
Intron |
|
|
NP_002284.3 |
View Full Product Details