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CATCTCACAGTGAATAGGTTGGCAG[A/G]TGTGGGCTGGCGGGTGGACTACACC
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 - 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 |
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 | 470 | Intron | NP_001271306.1 | |||
NM_001284378.1 | 470 | Intron | NP_001271307.1 | |||
NM_001284379.1 | 470 | Intron | NP_001271308.1 | |||
NM_001321844.1 | 470 | Missense Mutation | GAT,GGT | D,G 109 | NP_001308773.1 | |
NM_001321845.1 | 470 | Missense Mutation | GAT,GGT | D,G 87 | NP_001308774.1 | |
NM_001321846.1 | 470 | Intron | NP_001308775.1 | |||
NM_001321847.1 | 470 | Missense Mutation | GAT,GGT | D,G 111 | NP_001308776.1 | |
NM_001321848.1 | 470 | Missense Mutation | GAT,GGT | D,G 139 | NP_001308777.1 | |
NM_017828.4 | 470 | Missense Mutation | GAT,GGT | D,G 133 | NP_060298.2 | |
XM_005254509.3 | 470 | Missense Mutation | GAT,GGT | D,G 160 | XP_005254566.1 | |
XM_005254510.3 | 470 | Missense Mutation | GAT,GGT | D,G 138 | XP_005254567.1 | |
XM_011521739.1 | 470 | Missense Mutation | GAT,GGT | D,G 163 | XP_011520041.1 | |
XM_011521740.1 | 470 | Missense Mutation | GAT,GGT | D,G 141 | XP_011520042.1 | |
XM_011521741.1 | 470 | Intron | XP_011520043.1 | |||
XM_017022385.1 | 470 | Intron | XP_016877874.1 |
NEIL1 - nei like DNA glycosylase 1 | ||||||
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There are no transcripts associated with this gene. |