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CTCCCAGATCCGCCTGACTGCCTCC[C/T]ACCTGCCCACCTCTTCCCTCTGCAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616701 MIM: 608844 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
COMMD4 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
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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COMMD4 - COMM domain containing 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001284377.1 | Intron | NP_001271306.1 | ||||
NM_001284378.1 | Intron | NP_001271307.1 | ||||
NM_001284379.1 | Intron | NP_001271308.1 | ||||
NM_001321844.1 | Intron | NP_001308773.1 | ||||
NM_001321845.1 | Intron | NP_001308774.1 | ||||
NM_001321846.1 | Intron | NP_001308775.1 | ||||
NM_001321847.1 | Intron | NP_001308776.1 | ||||
NM_001321848.1 | Intron | NP_001308777.1 | ||||
NM_017828.4 | Intron | NP_060298.2 | ||||
XM_005254509.3 | Intron | XP_005254566.1 | ||||
XM_005254510.3 | Intron | XP_005254567.1 | ||||
XM_011521739.1 | Intron | XP_011520041.1 | ||||
XM_011521740.1 | Intron | XP_011520042.1 | ||||
XM_011521741.1 | Intron | XP_011520043.1 | ||||
XM_017022385.1 | Intron | XP_016877874.1 |
NEIL1 - nei like DNA glycosylase 1 | ||||||
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There are no transcripts associated with this gene. |