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- SNP ID:
- rs13108419
- Gene
-
PP12613TMEM155 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.4: 121766083 - 121766083 on Build GRCh38
- Polymorphism:
- A/G, Transition substitution
- Context Sequence [VIC/FAM]:
GGCTGGGTGATTCTGGTGTCGGGTT[A/G]CTCATGAGGCTCCGTTCAGATGTCA
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
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Literature Links: |
PP12613 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
|
|||||
AMR
|
| PP12613 - uncharacterized LOC100192379 | ||||||
|---|---|---|---|---|---|---|
| There are no transcripts associated with this gene. | ||||||
| TMEM155 - transmembrane protein 155 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001317837.1 | Intron | NP_001304766.1 | ||||
| NM_001317838.1 | Intron | NP_001304767.1 | ||||
| NM_001317839.1 | Intron | NP_001304768.1 | ||||
| NM_001317841.1 | Intron | NP_001304770.1 | ||||
| NM_001317842.1 | Intron | NP_001304771.1 | ||||
| NM_152399.3 | Intron | NP_689612.3 | ||||
| XM_005262737.2 | Intron | XP_005262794.1 | ||||
| XM_017007725.1 | Intron | XP_016863214.1 | ||||
| XM_017007726.1 | Intron | XP_016863215.1 | ||||
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