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- SNP ID:
- rs74702121
- Gene
-
KCNJ4LOC101927183 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.22: 38426919 - 38426919 on Build GRCh38
- Polymorphism:
- G/A, Transition substitution
- Context Sequence [VIC/FAM]:
GATGCCCGCCTCCTCCTTGGAACCC[G/A]CCTCCAGGCCCAGGCCTGCGGCCAC
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600504
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Literature Links: |
KCNJ4 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
| 1000Genome | Applied Biosystems® | HapMap |
|---|---|---|
| Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
| EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
| SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
| AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
| EUR - Not Available | ||
| AMR - Not Available |
| KCNJ4 - potassium voltage-gated channel subfamily J member 4 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_004981.1 | 1311 | Missense Mutation | GCG,GTG | A,V 405 | NP_004972.1 | |
| NM_152868.2 | 1311 | Missense Mutation | GCG,GTG | A,V 405 | NP_690607.1 | |
| LOC101927183 - uncharacterized LOC101927183 | ||||||
|---|---|---|---|---|---|---|
| There are no transcripts associated with this gene. | ||||||
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