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GCCGCGACGAGACGCACCGAGCACG[C/T]ATGTTCGCGCGCCACGACATCGTGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
18 submissions
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Phenotype: |
MIM: 616923 MIM: 180474 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
LOC102724450 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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LOC102724450 - uncharacterized LOC102724450 | ||||||
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There are no transcripts associated with this gene. |
RNF207 - ring finger protein 207 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_207396.2 | 579 | Silent Mutation | CGC,CGT | R,R 135 | NP_997279.2 | |
XM_011541439.2 | 579 | Silent Mutation | CGC,CGT | R,R 183 | XP_011539741.1 | |
XM_017001259.1 | 579 | Silent Mutation | CGC,CGT | R,R 135 | XP_016856748.1 |
RPL22 - ribosomal protein L22 | ||||||
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There are no transcripts associated with this gene. |