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CATTCTCAGGCGAAAGTGTCTCTTG[C/T]GTGCGTGGGCCGGAGGTTAGTGTGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605800 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CCDC97 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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CCDC97 - coiled-coil domain containing 97 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_052848.1 | 58 | UTR 5 | NP_443080.1 | |||
XM_005259377.4 | 58 | Intron | XP_005259434.1 | |||
XM_017027442.1 | 58 | Missense Mutation | GCG,GTG | A,V 33 | XP_016882931.1 |
HNRNPUL1 - heterogeneous nuclear ribonucleoprotein U like 1 | ||||||
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There are no transcripts associated with this gene. |