Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TAGGTGTACAAAGATAATCAATGCT[A/G]ATTCGGAGGACCCAAAATACATTAT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 154365 MIM: 604943 | ||||||||||||||||||||
Literature Links: |
PSMC2 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 |
PSMC2 - proteasome 26S subunit, ATPase 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001204453.1 | 622 | Missense Mutation | AAT,GAT | N,D 105 | NP_001191382.1 | |
NM_002803.3 | 622 | Missense Mutation | AAT,GAT | N,D 105 | NP_002794.1 | |
XM_005250505.1 | 622 | Missense Mutation | AAT,GAT | N,D 105 | XP_005250562.1 |
SLC26A5 - solute carrier family 26 member 5 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001167962.1 | 622 | Intron | NP_001161434.1 | |||
NM_001321787.1 | 622 | Intron | NP_001308716.1 | |||
NM_198999.2 | 622 | Intron | NP_945350.1 | |||
NM_206883.2 | 622 | Intron | NP_996766.1 | |||
NM_206884.2 | 622 | Intron | NP_996767.1 | |||
NM_206885.2 | 622 | Intron | NP_996768.1 | |||
XM_011516170.2 | 622 | Intron | XP_011514472.1 |