Product Details
- SNP ID
-
rs150404309
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.2:158172150 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- TACAGTAGACTCCATGTCCTTTCTT[A/G]GAGGTTTTTGAGGACTAATTTTTGG
- Phenotype
-
- Polymorphism
- A/G, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
CCDC148
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs17805784] 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
- CCDC148
- Gene Name
- coiled-coil domain containing 148
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_001301684.1 |
1988 |
Missense Mutation |
CCA,CTA |
P434L |
NP_001288613.1 |
| NM_001301685.1 |
1988 |
Intron |
|
|
NP_001288614.1 |
| NM_138803.3 |
1988 |
Missense Mutation |
CCA,CTA |
P580L |
NP_620158.3 |
| XM_005246319.3 |
1988 |
Missense Mutation |
CCA,CTA |
P601L |
XP_005246376.1 |
| XM_011510638.2 |
1988 |
Missense Mutation |
CCA,CTA |
P614L |
XP_011508940.1 |
| XM_017003392.1 |
1988 |
Missense Mutation |
CCA,CTA |
P593L |
XP_016858881.1 |
| XM_017003393.1 |
1988 |
Missense Mutation |
CCA,CTA |
P579L |
XP_016858882.1 |
| XM_017003394.1 |
1988 |
Missense Mutation |
CCA,CTA |
P540L |
XP_016858883.1 |
| XM_017003395.1 |
1988 |
Missense Mutation |
CCA,CTA |
P507L |
XP_016858884.1 |
| XM_017003396.1 |
1988 |
Missense Mutation |
CCA,CTA |
P494L |
XP_016858885.1 |
| XM_017003397.1 |
1988 |
Missense Mutation |
CCA,CTA |
P434L |
XP_016858886.1 |
| XM_017003398.1 |
1988 |
Missense Mutation |
CCA,CTA |
P367L |
XP_016858887.1 |
- Gene
- CCDC148-AS1
- Gene Name
- CCDC148 antisense RNA 1
There are no transcripts associated with this gene.
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