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- SNP ID:
- rs76766882
- Gene
-
PRMT7SLC7A6SLC7A6OS - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.16: 68301118 - 68301118 on Build GRCh38
- Polymorphism:
- T/G, Transversion substitution
- Context Sequence [VIC/FAM]:
AAAGACTCACTCCCCTAACATAAGT[T/G]TTCACTGTGGTGGGATGGTGCCGCC
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 610087
MIM: 605641
|
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Literature Links: |
PRMT7 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 |
| PRMT7 - protein arginine methyltransferase 7 | ||||||
|---|---|---|---|---|---|---|
| There are no transcripts associated with this gene. | ||||||
| SLC7A6 - solute carrier family 7 member 6 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001076785.2 | 1126 | UTR 3 | NP_001070253.1 | |||
| NM_003983.5 | 1126 | UTR 3 | NP_003974.3 | |||
| XM_011523433.1 | 1126 | UTR 3 | XP_011521735.1 | |||
| XM_011523434.1 | 1126 | UTR 3 | XP_011521736.1 | |||
| XM_011523438.1 | 1126 | UTR 3 | XP_011521740.1 | |||
| XM_011523439.1 | 1126 | UTR 3 | XP_011521741.1 | |||
| XM_017023851.1 | 1126 | UTR 3 | XP_016879340.1 | |||
| SLC7A6OS - solute carrier family 7 member 6 opposite strand | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_032178.2 | 1126 | UTR 3 | NP_115554.2 | |||
| XM_011523372.2 | 1126 | Intron | XP_011521674.1 | |||
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