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GTCCTACCTGCTGTGGGGTAGGTTC[A/G]GGTGCCCGGTTTGCCAGGCGGCTGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603277 MIM: 164031 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CHD4 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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CHD4 - chromodomain helicase DNA binding protein 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001273.3 | 5807 | Silent Mutation | CCC,CCT | P,P 1901 | NP_001264.2 | |
NM_001297553.1 | 5807 | Silent Mutation | CCC,CCT | P,P 1894 | NP_001284482.1 | |
XM_005253668.3 | 5807 | Silent Mutation | CCC,CCT | P,P 1894 | XP_005253725.1 | |
XM_006718958.1 | 5807 | Silent Mutation | CCC,CCT | P,P 1929 | XP_006719021.1 | |
XM_006718959.1 | 5807 | Silent Mutation | CCC,CCT | P,P 1904 | XP_006719022.1 | |
XM_006718960.1 | 5807 | Silent Mutation | CCC,CCT | P,P 1903 | XP_006719023.1 | |
XM_006718961.2 | 5807 | Silent Mutation | CCC,CCT | P,P 1897 | XP_006719024.1 | |
XM_006718962.1 | 5807 | Silent Mutation | CCC,CCT | P,P 1891 | XP_006719025.1 | |
XM_017018725.1 | 5807 | Silent Mutation | CCC,CCT | P,P 1903 | XP_016874214.1 | |
XM_017018726.1 | 5807 | Silent Mutation | CCC,CCT | P,P 1902 | XP_016874215.1 | |
XM_017018727.1 | 5807 | Silent Mutation | CCC,CCT | P,P 1901 | XP_016874216.1 | |
XM_017018728.1 | 5807 | Silent Mutation | CCC,CCT | P,P 1900 | XP_016874217.1 | |
XM_017018729.1 | 5807 | Silent Mutation | CCC,CCT | P,P 1895 | XP_016874218.1 | |
XM_017018730.1 | 5807 | Silent Mutation | CCC,CCT | P,P 1889 | XP_016874219.1 | |
XM_017018731.1 | 5807 | Silent Mutation | CCC,CCT | P,P 1888 | XP_016874220.1 | |
XM_017018732.1 | 5807 | Silent Mutation | CCC,CCT | P,P 1884 | XP_016874221.1 | |
XM_017018733.1 | 5807 | Silent Mutation | CCC,CCT | P,P 1882 | XP_016874222.1 | |
XM_017018734.1 | 5807 | Silent Mutation | CCC,CCT | P,P 1881 | XP_016874223.1 |
NOP2 - NOP2 nucleolar protein | ||||||
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There are no transcripts associated with this gene. |