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- SNP ID:
- rs79333548
- Gene
-
TMEM175 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.4: 945519 - 945519 on Build GRCh38
- Polymorphism:
- G/A, Transition substitution
- Context Sequence [VIC/FAM]:
TTGCACCTCCCCGATCTCCCTGATT[G/A]CTAGTGAAGTGGAATGCCTTGTGTG
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 616660
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Literature Links: |
TMEM175 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
| 1000Genome | Applied Biosystems® | HapMap | |||
|---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
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AMR
|
| TMEM175 - transmembrane protein 175 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001297423.1 | Intron | NP_001284352.1 | ||||
| NM_001297424.1 | Intron | NP_001284353.1 | ||||
| NM_001297425.1 | Intron | NP_001284354.1 | ||||
| NM_001297426.1 | Intron | NP_001284355.1 | ||||
| NM_001297427.1 | Intron | NP_001284356.1 | ||||
| NM_001297428.1 | Intron | NP_001284357.1 | ||||
| NM_032326.3 | Intron | NP_115702.1 | ||||
| XM_005272301.2 | Intron | XP_005272358.1 | ||||
| XM_005272303.4 | Intron | XP_005272360.1 | ||||
| XM_005272304.1 | Intron | XP_005272361.1 | ||||
| XM_005272307.4 | Intron | XP_005272364.1 | ||||
| XM_011513576.1 | Intron | XP_011511878.1 | ||||
| XM_017008701.1 | Intron | XP_016864190.1 | ||||
| XM_017008702.1 | Intron | XP_016864191.1 | ||||
| XM_017008703.1 | Intron | XP_016864192.1 | ||||
| XM_017008704.1 | Intron | XP_016864193.1 | ||||
| XM_017008705.1 | Intron | XP_016864194.1 | ||||
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