Product Details
- SNP ID
-
rs148471769
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.4:17577532 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CCGACGTCTGGCCGTGAGACGTTTC[C/G]GGAGCCGGAGTCTCTCCACCGCAGA
- Phenotype
-
MIM: 170250
- Polymorphism
- C/G, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
LAP3
PubMed Links
Gene Details
- Gene
- LAP3
- Gene Name
- leucine aminopeptidase 3
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_015907.2 |
229 |
Missense Mutation |
CGG,GGG |
R23G |
NP_056991.2 |
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