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- SNP ID:
- rs144206402
- Gene
-
SP4 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.7: 21429537 - 21429537 on Build GRCh38
- Polymorphism:
- A/G, Transition substitution
- Context Sequence [VIC/FAM]:
ACGTTTCTCAACCAGCCTCTAGTTC[A/G]TCTAGTTCTTCCAGCAGTAATAACG
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600540
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Literature Links: |
SP4 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 |
| SP4 - Sp4 transcription factor | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001326542.1 | 590 | Silent Mutation | TCA,TCG | S,S 107 | NP_001313471.1 | |
| NM_001326543.1 | 590 | UTR 5 | NP_001313472.1 | |||
| NM_003112.4 | 590 | Silent Mutation | TCA,TCG | S,S 124 | NP_003103.2 | |
| XM_005249828.2 | 590 | Silent Mutation | TCA,TCG | S,S 107 | XP_005249885.1 | |
| XM_005249829.3 | 590 | Silent Mutation | TCA,TCG | S,S 124 | XP_005249886.1 | |
| XM_011515486.2 | 590 | Silent Mutation | TCA,TCG | S,S 124 | XP_011513788.1 | |
| XM_011515487.2 | 590 | Silent Mutation | TCA,TCG | S,S 124 | XP_011513789.1 | |
| XM_011515489.2 | 590 | Silent Mutation | TCA,TCG | S,S 124 | XP_011513791.1 | |
| XM_017012557.1 | 590 | Silent Mutation | TCA,TCG | S,S 124 | XP_016868046.1 | |
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