Product Details
- SNP ID
-
rs138357678
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.10:97001264 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GGGCACGAGCCCCGGCACTCCACCC[A/G]TGACAGGGGGCGCGTGGTCTGGCAG
- Phenotype
-
MIM: 603742
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
SLIT1
PubMed Links
Gene Details
- Gene
- SLIT1
- Gene Name
- slit guidance ligand 1
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_003061.2 |
4705 |
Missense Mutation |
CGG,TGG |
R1485W |
NP_003052.2 |
View Full Product Details