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CCCCCTGGTGCCATTGGGCAAGGCA[A/G]GCCAGAGAGGCCAGGGGCAGCTGGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
2 submissions
|
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Phenotype: |
MIM: 616775 | ||||||||||||||||||||
Literature Links: |
AIM1L 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 |
AIM1L - absent in melanoma 1-like | ||||||
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There are no transcripts associated with this gene. |
ZNF683 - zinc finger protein 683 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001114759.2 | 1655 | Silent Mutation | GCC,GCT | A,A 446 | NP_001108231.1 | |
NM_001307925.1 | 1655 | Silent Mutation | GCC,GCT | A,A 466 | NP_001294854.1 | |
NM_173574.3 | 1655 | Silent Mutation | GCC,GCT | A,A 446 | NP_775845.2 | |
XM_005245828.3 | 1655 | Silent Mutation | GCC,GCT | A,A 474 | XP_005245885.1 | |
XM_005245830.3 | 1655 | Silent Mutation | GCC,GCT | A,A 466 | XP_005245887.1 | |
XM_005245832.3 | 1655 | Silent Mutation | GCC,GCT | A,A 466 | XP_005245889.1 | |
XM_006710555.3 | 1655 | Silent Mutation | GCC,GCT | A,A 475 | XP_006710618.1 | |
XM_011541198.2 | 1655 | Silent Mutation | GCC,GCT | A,A 466 | XP_011539500.1 | |
XM_017000954.1 | 1655 | Silent Mutation | GCC,GCT | A,A 475 | XP_016856443.1 | |
XM_017000955.1 | 1655 | Silent Mutation | GCC,GCT | A,A 475 | XP_016856444.1 | |
XM_017000956.1 | 1655 | Silent Mutation | GCC,GCT | A,A 474 | XP_016856445.1 | |
XM_017000957.1 | 1655 | Silent Mutation | GCC,GCT | A,A 455 | XP_016856446.1 | |
XM_017000958.1 | 1655 | UTR 3 | XP_016856447.1 | |||
XM_017000959.1 | 1655 | UTR 3 | XP_016856448.1 |