Search Thermo Fisher Scientific
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ACCAGTGCCAGGCTGGAAAGGATAC[A/G]ACTGATGCTTCAACAAGTGTTTCCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
CUEDC1 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 |
CUEDC1 - CUE domain containing 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001271875.1 | 836 | Missense Mutation | TCG,TTG | S,L 345 | NP_001258804.1 | |
NM_001292025.1 | 836 | Missense Mutation | TCG,TTG | S,L 345 | NP_001278954.1 | |
XM_006721900.2 | 836 | Missense Mutation | TCG,TTG | S,L 345 | XP_006721963.1 | |
XM_011524812.2 | 836 | Missense Mutation | TCG,TTG | S,L 238 | XP_011523114.1 | |
XM_017024640.1 | 836 | Missense Mutation | TCG,TTG | S,L 317 | XP_016880129.1 | |
XM_017024641.1 | 836 | Missense Mutation | TCG,TTG | S,L 263 | XP_016880130.1 |