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TTCATTTACTGACTTCAGATTGGGG[G/T]ACCTGAAGTGAAAAAGCAAACATAA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607599 MIM: 604166 | ||||||||||||||||||||
Literature Links: |
C8orf89 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
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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 |
C8orf89 - chromosome 8 open reading frame 89 | ||||||
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There are no transcripts associated with this gene. |
RDH10 - retinol dehydrogenase 10 (all-trans) | ||||||
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There are no transcripts associated with this gene. |
RPL7 - ribosomal protein L7 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000971.3 | 1046 | Intron | NP_000962.2 | |||
XM_006716463.2 | 1046 | Missense Mutation | TAC,TCC | Y,S 104 | XP_006716526.1 |