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TCACTCTGAAAGACTTCTTCATGGT[A/G]GATTTGCCCTTGCCCGGCAATTTTA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
1 submissions
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Phenotype: |
MIM: 616072 | ||||||||||||||||||||
Literature Links: |
HP1BP3 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 |
HP1BP3 - heterochromatin protein 1 binding protein 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_016287.3 | 2205 | Silent Mutation | TCC,TCT | S,S 543 | NP_057371.2 | |
XM_005245875.4 | 2205 | Silent Mutation | TCC,TCT | S,S 543 | XP_005245932.1 | |
XM_005245876.3 | 2205 | Silent Mutation | TCC,TCT | S,S 543 | XP_005245933.1 | |
XM_005245877.4 | 2205 | Silent Mutation | TCC,TCT | S,S 543 | XP_005245934.1 | |
XM_005245878.4 | 2205 | Silent Mutation | TCC,TCT | S,S 543 | XP_005245935.1 | |
XM_005245879.4 | 2205 | Silent Mutation | TCC,TCT | S,S 505 | XP_005245936.1 | |
XM_011541532.1 | 2205 | Silent Mutation | TCC,TCT | S,S 505 | XP_011539834.1 | |
XM_011541533.1 | 2205 | Silent Mutation | TCC,TCT | S,S 505 | XP_011539835.1 | |
XM_011541534.2 | 2205 | Silent Mutation | TCC,TCT | S,S 505 | XP_011539836.1 | |
XM_017001393.1 | 2205 | Silent Mutation | TCC,TCT | S,S 543 | XP_016856882.1 | |
XM_017001394.1 | 2205 | Silent Mutation | TCC,TCT | S,S 505 | XP_016856883.1 |