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AAATCCAAGCTTTGCAACTTACGTA[A/G]CCTTCCCCCACAAGCCCTCATTGAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602000 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
LOC105373562 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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LOC105373562 - uncharacterized LOC105373562 | ||||||
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There are no transcripts associated with this gene. |
POLR1B - RNA polymerase I subunit B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001137604.2 | 679 | Missense Mutation | AAC,AGC | N,S 94 | NP_001131076.1 | |
NM_001282772.1 | 679 | Missense Mutation | AAC,AGC | N,S 188 | NP_001269701.1 | |
NM_001282774.1 | 679 | Missense Mutation | AAC,AGC | N,S 150 | NP_001269703.1 | |
NM_001282776.1 | 679 | Intron | NP_001269705.1 | |||
NM_001282777.1 | 679 | Missense Mutation | AAC,AGC | N,S 11 | NP_001269706.1 | |
NM_001282779.1 | 679 | Missense Mutation | AAC,AGC | N,S 11 | NP_001269708.1 | |
NM_019014.5 | 679 | Missense Mutation | AAC,AGC | N,S 150 | NP_061887.2 |