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TGCGGCGGCCGAGCTCCAAGACTGC[A/G]CGCACCTCTTCAGCCACGTCCTGCC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608213 MIM: 605247 MIM: 609302 | ||||||||||||||||||||
Literature Links: |
CEND1 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 |
CEND1 - cell cycle exit and neuronal differentiation 1 | ||||||
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There are no transcripts associated with this gene. |
PANO1 - proapoptotic nucleolar protein 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001293167.1 | 3767 | Intron | NP_001280096.1 |
PIDD1 - p53-induced death domain protein 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_145886.3 | 3767 | Silent Mutation | CGC,CGT | R,R 870 | NP_665893.2 | |
NM_145887.3 | 3767 | Silent Mutation | CGC,CGT | R,R 853 | NP_665894.2 | |
XM_005253005.4 | 3767 | Silent Mutation | CGC,CGT | R,R 894 | XP_005253062.1 | |
XM_005253006.4 | 3767 | Silent Mutation | CGC,CGT | R,R 894 | XP_005253063.1 | |
XM_005253007.3 | 3767 | Silent Mutation | CGC,CGT | R,R 894 | XP_005253064.1 | |
XM_005253008.4 | 3767 | Silent Mutation | CGC,CGT | R,R 748 | XP_005253065.1 | |
XM_011520209.2 | 3767 | Silent Mutation | CGC,CGT | R,R 880 | XP_011518511.1 | |
XM_011520210.2 | 3767 | Silent Mutation | CGC,CGT | R,R 870 | XP_011518512.1 | |
XM_011520211.2 | 3767 | Silent Mutation | CGC,CGT | R,R 853 | XP_011518513.1 | |
XM_011520212.1 | 3767 | Silent Mutation | CGC,CGT | R,R 748 | XP_011518514.1 | |
XM_011520213.2 | 3767 | Silent Mutation | CGC,CGT | R,R 581 | XP_011518515.1 | |
XM_017017993.1 | 3767 | Silent Mutation | CGC,CGT | R,R 557 | XP_016873482.1 |
SLC25A22 - solute carrier family 25 member 22 | ||||||
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There are no transcripts associated with this gene. |