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AGTCTGAAATTTGAGAGGATAACTT[C/T]GTCTTGGCTGCTGTTTGTTGCTGTA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 613367 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
LIN54 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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LIN54 - lin-54 DREAM MuvB core complex component | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001115007.2 | 1905 | Silent Mutation | ACA,ACG | T,T 439 | NP_001108479.1 | |
NM_001115008.2 | 1905 | Silent Mutation | ACA,ACG | T,T 439 | NP_001108480.1 | |
NM_001288996.1 | 1905 | Silent Mutation | ACA,ACG | T,T 571 | NP_001275925.1 | |
NM_001288997.1 | 1905 | Silent Mutation | ACA,ACG | T,T 439 | NP_001275926.1 | |
NM_194282.3 | 1905 | Silent Mutation | ACA,ACG | T,T 660 | NP_919258.2 | |
XM_005262750.4 | 1905 | Silent Mutation | ACA,ACG | T,T 660 | XP_005262807.1 | |
XM_006714081.3 | 1905 | Silent Mutation | ACA,ACG | T,T 660 | XP_006714144.1 | |
XM_017007728.1 | 1905 | Silent Mutation | ACA,ACG | T,T 571 | XP_016863217.1 | |
XM_017007729.1 | 1905 | Silent Mutation | ACA,ACG | T,T 259 | XP_016863218.1 | |
XM_017007730.1 | 1905 | Silent Mutation | ACA,ACG | T,T 259 | XP_016863219.1 |