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GCACCTGGATGGAGTCCACCCTCTG[C/T]GGGGCGGGCGGCGGGTTGTCTCCCC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616704 MIM: 605885 | ||||||||||||||||||||
Literature Links: |
COMMD10 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 |
COMMD10 - COMM domain containing 10 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001308080.1 | 3669 | Intron | NP_001295009.1 | |||
NM_016144.3 | 3669 | Intron | NP_057228.1 | |||
XM_011543458.2 | 3669 | Intron | XP_011541760.1 | |||
XM_011543460.2 | 3669 | Intron | XP_011541762.1 | |||
XM_017009553.1 | 3669 | Intron | XP_016865042.1 | |||
XM_017009555.1 | 3669 | Intron | XP_016865044.1 | |||
XM_017009556.1 | 3669 | Intron | XP_016865045.1 | |||
XM_017009557.1 | 3669 | Intron | XP_016865046.1 |
SEMA6A - semaphorin 6A | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001300780.1 | 3669 | Silent Mutation | CCA,CCG | P,P 980 | NP_001287709.1 | |
NM_020796.4 | 3669 | Silent Mutation | CCA,CCG | P,P 963 | NP_065847.1 | |
XM_005272042.3 | 3669 | Silent Mutation | CCA,CCG | P,P 908 | XP_005272099.2 | |
XM_006714663.1 | 3669 | Silent Mutation | CCA,CCG | P,P 985 | XP_006714726.1 | |
XM_017009675.1 | 3669 | Silent Mutation | CCA,CCG | P,P 985 | XP_016865164.1 | |
XM_017009676.1 | 3669 | Silent Mutation | CCA,CCG | P,P 837 | XP_016865165.1 |
SEMA6A-AS1 - SEMA6A antisense RNA 1 | ||||||
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There are no transcripts associated with this gene. |