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GGAGTCAGAGGGGACAGGGTTGCCA[C/T]GGGGAATGGAAGAGCAAAGCGGTGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616167 MIM: 614709 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
DCUN1D3 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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DCUN1D3 - defective in cullin neddylation 1 domain containing 3 | ||||||
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There are no transcripts associated with this gene. |
LYRM1 - LYR motif containing 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001128301.2 | Intron | NP_001121773.1 | ||||
NM_001128302.2 | Intron | NP_001121774.1 | ||||
NM_001302835.1 | Intron | NP_001289764.1 | ||||
NM_001302836.1 | Intron | NP_001289765.1 | ||||
NM_020424.4 | Intron | NP_065157.1 | ||||
XM_005255444.1 | Intron | XP_005255501.1 | ||||
XM_011545900.2 | Intron | XP_011544202.1 | ||||
XM_011545901.2 | Intron | XP_011544203.1 | ||||
XM_011545902.1 | Intron | XP_011544204.1 | ||||
XM_011545908.2 | Intron | XP_011544210.1 | ||||
XM_017023475.1 | Intron | XP_016878964.1 | ||||
XM_017023476.1 | Intron | XP_016878965.1 | ||||
XM_017023477.1 | Intron | XP_016878966.1 | ||||
XM_017023478.1 | Intron | XP_016878967.1 | ||||
XM_017023479.1 | Intron | XP_016878968.1 | ||||
XM_017023480.1 | Intron | XP_016878969.1 | ||||
XM_017023481.1 | Intron | XP_016878970.1 | ||||
XM_017023482.1 | Intron | XP_016878971.1 |