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Species: |
Human | ||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606607 MIM: 606472 | ||||||||||||||||||||||||||||||||
Literature Links: |
LSM14B PubMed Links | ||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global - Not Available | Caucasian - Not Available | CEPH (CEU)
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EAS - Not Available | African American - Not Available | YRI (Yoruba)
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SAS - Not Available | Chinese - Not Available | JPT (Japanese)
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AFR - Not Available | Japanese - Not Available | CHB (Han Chinese)
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EUR - Not Available | |||||
AMR - Not Available |
LSM14B - LSM family member 14B | ||||||
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There are no transcripts associated with this gene. |
PSMA7 - proteasome subunit alpha 7 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_002792.3 | 529 | Missense Mutation | AAG,AGG | K,R 125 | NP_002783.1 |
SS18L1 - SS18L1, nBAF chromatin remodeling complex subunit | ||||||
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There are no transcripts associated with this gene. |
Set Membership: |
HapMap |