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- SNP ID:
- rs79651379
- Gene
-
GPR151TCERG1 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.5: 146509180 - 146509180 on Build GRCh38
- Polymorphism:
- A/C, Transversion substitution
- Context Sequence [VIC/FAM]:
GAGAATTTGAAGAATATATCAGAGA[A/C]AAATATATCACAGCCAAAGCTGACT
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605409
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Literature Links: |
GPR151 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 |
| GPR151 - G protein-coupled receptor 151 | ||||||
|---|---|---|---|---|---|---|
| There are no transcripts associated with this gene. | ||||||
| TCERG1 - transcription elongation regulator 1 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001040006.1 | 3307 | Missense Mutation | GAA,GAC | E,D 989 | NP_001035095.1 | |
| NM_006706.3 | 3307 | Missense Mutation | GAA,GAC | E,D 1010 | NP_006697.2 | |
| XM_005268365.2 | 3307 | Missense Mutation | GAA,GAC | E,D 1027 | XP_005268422.1 | |
| XM_017008977.1 | 3307 | Missense Mutation | GAA,GAC | E,D 1006 | XP_016864466.1 | |
| XM_017008978.1 | 3307 | Missense Mutation | GAA,GAC | E,D 966 | XP_016864467.1 | |
| XM_017008979.1 | 3307 | Missense Mutation | GAA,GAC | E,D 949 | XP_016864468.1 | |
| XM_017008980.1 | 3307 | Intron | XP_016864469.1 | |||
| XM_017008981.1 | 3307 | Missense Mutation | GAA,GAC | E,D 736 | XP_016864470.1 | |
| XM_017008982.1 | 3307 | Missense Mutation | GAA,GAC | E,D 732 | XP_016864471.1 | |
| XM_017008983.1 | 3307 | Missense Mutation | GAA,GAC | E,D 715 | XP_016864472.1 | |
| XM_017008984.1 | 3307 | Intron | XP_016864473.1 | |||
| XM_017008985.1 | 3307 | Intron | XP_016864474.1 | |||
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