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- SNP ID:
- rs77258715
- Gene
-
TSEN2 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.3: 12489908 - 12489908 on Build GRCh38
- Polymorphism:
- A/G, Transition substitution
- Context Sequence [VIC/FAM]:
GTCAGGACCATGGTCCTCTGAAAGA[A/G]TTCAAGATATTCCGTGCTGAAATGA
Genomic Map
Back To TopAssay Details
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608753
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Literature Links: |
TSEN2 PubMed Links | |||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
| 1000Genome | Applied Biosystems® | HapMap | |||
|---|---|---|---|---|---|
Global
|
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 |
| TSEN2 - tRNA splicing endonuclease subunit 2 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001145392.1 | 425 | Intron | NP_001138864.1 | |||
| NM_001145393.2 | 425 | Intron | NP_001138865.1 | |||
| NM_001145394.1 | 425 | Intron | NP_001138866.1 | |||
| NM_001321277.1 | 425 | Intron | NP_001308206.1 | |||
| NM_001321278.1 | 425 | Silent Mutation | GAA,GAG | E,E 36 | NP_001308207.1 | |
| NM_001321279.1 | 425 | Silent Mutation | GAA,GAG | E,E 36 | NP_001308208.1 | |
| NM_025265.3 | 425 | Silent Mutation | GAA,GAG | E,E 36 | NP_079541.1 | |
| XM_011534139.2 | 425 | Intron | XP_011532441.1 | |||
| XM_017007292.1 | 425 | Intron | XP_016862781.1 | |||
| XM_017007293.1 | 425 | Silent Mutation | GAA,GAG | E,E 36 | XP_016862782.1 | |
| XM_017007294.1 | 425 | Intron | XP_016862783.1 | |||
| XM_017007295.1 | 425 | Silent Mutation | GAA,GAG | E,E 36 | XP_016862784.1 | |
| XM_017007296.1 | 425 | Silent Mutation | GAA,GAG | E,E 36 | XP_016862785.1 | |
| XM_017007297.1 | 425 | Silent Mutation | GAA,GAG | E,E 36 | XP_016862786.1 | |
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