Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GAATGTGAAACTGATCCCTCTCCTA[C/G]TTTATCTTCTTTTTCCTGTGCTGTA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 614693 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
ATMIN 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)
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EAS
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African American - Not Available | YRI (Yoruba)
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SAS
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Chinese - Not Available | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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ATMIN - ATM interactor | ||||||
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There are no transcripts associated with this gene. |
C16orf46 - chromosome 16 open reading frame 46 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001100873.1 | 1684 | Missense Mutation | AAC,AAG | N,K 388 | NP_001094343.1 | |
NM_152337.2 | 1684 | Intron | NP_689550.2 | |||
XM_005255792.2 | 1684 | Missense Mutation | AAC,AAG | N,K 388 | XP_005255849.1 | |
XM_011522848.2 | 1684 | UTR 3 | XP_011521150.2 | |||
XM_011522849.2 | 1684 | UTR 3 | XP_011521151.2 | |||
XM_017022916.1 | 1684 | UTR 3 | XP_016878405.1 | |||
XM_017022917.1 | 1684 | UTR 3 | XP_016878406.1 |