Product Details
- SNP ID
-
rs202024343
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.18:48029412 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- AGCGCGAAGGCCAGGAGGCCCCCCG[C/G]GTTCCTCTCAGCCTCCAGCTGCGCG
- Phenotype
-
MIM: 616591
- Polymorphism
- C/G, Transversion Substitution
- Allele Nomenclature
-
- Literature Links
-
ZBTB7C
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs7231151] are located under a primer 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
- ZBTB7C
- Gene Name
- zinc finger and BTB domain containing 7C
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001039360.2 |
2421 |
Missense Mutation |
CCG,GCG |
P570A |
NP_001034449.1 |
NM_001318841.1 |
2421 |
Missense Mutation |
CCG,GCG |
P570A |
NP_001305770.1 |
XM_005258229.4 |
2421 |
Missense Mutation |
CCG,GCG |
P570A |
XP_005258286.1 |
XM_011525861.2 |
2421 |
Missense Mutation |
CCG,GCG |
P619A |
XP_011524163.1 |
XM_011525863.2 |
2421 |
Missense Mutation |
CCG,GCG |
P579A |
XP_011524165.1 |
XM_011525864.2 |
2421 |
Missense Mutation |
CCG,GCG |
P579A |
XP_011524166.1 |
XM_011525865.2 |
2421 |
Missense Mutation |
CCG,GCG |
P579A |
XP_011524167.1 |
XM_011525866.2 |
2421 |
Missense Mutation |
CCG,GCG |
P579A |
XP_011524168.1 |
XM_011525867.2 |
2421 |
Missense Mutation |
CCG,GCG |
P579A |
XP_011524169.1 |
XM_011525869.2 |
2421 |
Missense Mutation |
CCG,GCG |
P578A |
XP_011524171.1 |
XM_011525870.2 |
2421 |
Missense Mutation |
CCG,GCG |
P570A |
XP_011524172.1 |
XM_011525871.2 |
2421 |
Missense Mutation |
CCG,GCG |
P570A |
XP_011524173.1 |
XM_017025605.1 |
2421 |
Missense Mutation |
CCG,GCG |
P619A |
XP_016881094.1 |
XM_017025606.1 |
2421 |
Missense Mutation |
CCG,GCG |
P579A |
XP_016881095.1 |
XM_017025607.1 |
2421 |
Missense Mutation |
CCG,GCG |
P579A |
XP_016881096.1 |
XM_017025608.1 |
2421 |
Missense Mutation |
CCG,GCG |
P578A |
XP_016881097.1 |
XM_017025609.1 |
2421 |
Missense Mutation |
CCG,GCG |
P570A |
XP_016881098.1 |
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