Product Details
- SNP ID
-
rs150401209
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.3:195568911 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CCTGTAGAACCTGGTTACGAGAGCT[C/T]GGGGCAGTTCACCTGGTCTGTGACC
- Phenotype
-
MIM: 107740
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
APOD
PubMed Links
Gene Details
- Gene
- APOD
- Gene Name
- apolipoprotein D
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001647.3 |
921 |
Missense Mutation |
AAG,GAG |
K187E |
NP_001638.1 |
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