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CCCCAAAGCACCTGACATGCCTGTT[C/T]TGCTCTTTGATCCGTGTGGTTCATA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606607 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
LSM14B PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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LSM14B - LSM family member 14B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_144703.2 | Intron | NP_653304.2 | ||||
XM_005260302.3 | Intron | XP_005260359.1 | ||||
XM_011528605.2 | Intron | XP_011526907.1 | ||||
XM_011528606.2 | Intron | XP_011526908.1 | ||||
XM_011528607.2 | Intron | XP_011526909.1 | ||||
XM_011528608.2 | Intron | XP_011526910.1 | ||||
XM_011528609.2 | Intron | XP_011526911.1 | ||||
XM_011528611.2 | Intron | XP_011526913.1 | ||||
XM_011528612.2 | Intron | XP_011526914.1 | ||||
XM_011528613.2 | Intron | XP_011526915.1 | ||||
XM_011528614.2 | Intron | XP_011526916.1 | ||||
XM_011528615.2 | Intron | XP_011526917.1 | ||||
XM_017027688.1 | Intron | XP_016883177.1 | ||||
XM_017027689.1 | Intron | XP_016883178.1 | ||||
XM_017027690.1 | Intron | XP_016883179.1 |
PSMA7 - proteasome subunit alpha 7 | ||||||
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There are no transcripts associated with this gene. |