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TTTTTCTAGGAAAGTATGTGATGGT[C/G]ATGGGAGTGGTTCAGGCCTGCAGCC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 612426 | ||||||||||||||||||||
Literature Links: |
LOC105371083 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 |
LOC105371083 - uncharacterized LOC105371083 | ||||||
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There are no transcripts associated with this gene. |
RMI2 - RecQ mediated genome instability 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_152308.2 | 346 | Silent Mutation | GTC,GTG | V,V 104 | NP_689521.1 |