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GTGCCTGATGTGTTCCAACAGATGC[A/G]GGAGCTGGGCCTGGCTCGGCGGGTG
Species: |
Human | |||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611200 | |||||||||||||||||||||||||||||
Literature Links: |
LOC101926934 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)
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EAS - Not Available | African American - Not Available | YRI (Yoruba)
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SAS - Not Available | Chinese - Not Available | CHB (Han Chinese)
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AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR - Not Available | |||||
AMR - Not Available |
LOC101926934 - uncharacterized LOC101926934 | ||||||
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There are no transcripts associated with this gene. |
TDRD6 - tudor domain containing 6 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001010870.2 | 829 | Missense Mutation | CAG,CGG | Q,R 192 | NP_001010870.1 | |
NM_001168359.1 | 829 | Missense Mutation | CAG,CGG | Q,R 192 | NP_001161831.1 |
Set Membership: |
HapMap |