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AGTGACACTTTGGTTATCACTTGAT[C/T]AGAAAAATACTCGTCCCAGCTCAAA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 614917 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
RMND1 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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RMND1 - required for meiotic nuclear division 1 homolog | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001271937.1 | 1529 | Silent Mutation | NP_001258866.1 | |||
NM_017909.3 | 1529 | Silent Mutation | NP_060379.2 | |||
XM_005267040.3 | 1529 | Silent Mutation | XP_005267097.1 | |||
XM_017010988.1 | 1529 | Silent Mutation | XP_016866477.1 |