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CACCTCCGGGGCTGAAAATGCAGCA[G/T]TGAGTGCTATGCTGCACGCTGTAGC
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 |
---|---|---|
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 |
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 | 309 | Missense Mutation | GTG,TTG | V,L 63 | NP_443080.1 | |
XM_005259377.4 | 309 | UTR 5 | XP_005259434.1 | |||
XM_017027442.1 | 309 | Missense Mutation | GTG,TTG | V,L 117 | XP_016882931.1 |
HNRNPUL1 - heterogeneous nuclear ribonucleoprotein U like 1 | ||||||
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There are no transcripts associated with this gene. |