Product Details
- SNP ID
-
rs200149481
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.21:36036232 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- TAGTTGGTTTATCAGGGCCTCTTTT[G/T]CATCCTTCATATGAGACACCTGAAA
- Phenotype
-
- Polymorphism
- G/T, Transversion Substitution
- Allele Nomenclature
-
- Literature Links
-
SETD4
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs68024241] 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
- SETD4
- Gene Name
- SET domain containing 4
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001007259.2 |
1415 |
Intron |
|
|
NP_001007260.1 |
NM_001007261.2 |
1415 |
Intron |
|
|
NP_001007262.1 |
NM_001286752.1 |
1415 |
Missense Mutation |
GAA,GCA |
E379A |
NP_001273681.1 |
NM_017438.4 |
1415 |
Missense Mutation |
GAA,GCA |
E403A |
NP_059134.1 |
XM_011529636.1 |
1415 |
Missense Mutation |
GAA,GCA |
E403A |
XP_011527938.1 |
XM_011529637.1 |
1415 |
Missense Mutation |
GAA,GCA |
E403A |
XP_011527939.1 |
XM_011529638.2 |
1415 |
Missense Mutation |
GAA,GCA |
E403A |
XP_011527940.1 |
XM_011529639.1 |
1415 |
Missense Mutation |
GAA,GCA |
E403A |
XP_011527941.1 |
XM_011529640.2 |
1415 |
Missense Mutation |
GAA,GCA |
E403A |
XP_011527942.1 |
XM_011529642.1 |
1415 |
Missense Mutation |
GAA,GCA |
E379A |
XP_011527944.1 |
XM_011529643.1 |
1415 |
Missense Mutation |
GAA,GCA |
E379A |
XP_011527945.1 |
XM_011529644.1 |
1415 |
Missense Mutation |
GAA,GCA |
E379A |
XP_011527946.1 |
XM_017028403.1 |
1415 |
Missense Mutation |
GAA,GCA |
E403A |
XP_016883892.1 |
XM_017028404.1 |
1415 |
Missense Mutation |
GAA,GCA |
E379A |
XP_016883893.1 |
XM_017028405.1 |
1415 |
Intron |
|
|
XP_016883894.1 |
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