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- SNP ID:
- rs77840707
- Gene
-
PSMC2SLC26A5 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.7: 103356415 - 103356415 on Build GRCh38
- Polymorphism:
- A/G, Transition substitution
- Context Sequence [VIC/FAM]:
GGGGTCAAAGATATTATAGTTTTAA[A/G]ATCCTGTGAAAATTACTTTGGCCAG
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 154365
MIM: 604943
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Literature Links: |
PSMC2 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
|
| PSMC2 - proteasome 26S subunit, ATPase 2 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001204453.1 | Intron | NP_001191382.1 | ||||
| NM_002803.3 | Intron | NP_002794.1 | ||||
| XM_005250505.1 | Intron | XP_005250562.1 | ||||
| SLC26A5 - solute carrier family 26 member 5 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001167962.1 | Intron | NP_001161434.1 | ||||
| NM_001321787.1 | Intron | NP_001308716.1 | ||||
| NM_198999.2 | Intron | NP_945350.1 | ||||
| NM_206883.2 | Intron | NP_996766.1 | ||||
| NM_206884.2 | Intron | NP_996767.1 | ||||
| NM_206885.2 | Intron | NP_996768.1 | ||||
| XM_011516170.2 | Intron | XP_011514472.1 | ||||
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