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- SNP ID:
- rs28368727
- Gene
-
HERC6 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.4: 88382673 - 88382673 on Build GRCh38
- Polymorphism:
- A/G, Transition substitution
- Context Sequence [VIC/FAM]:
AGTCAATTTGAACATTCAGCAGTTC[A/G]TGAATTGAGCAGCACCAGACCTCAA
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 609249
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Literature Links: |
HERC6 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
| 1000Genome | Applied Biosystems® | HapMap | |||
|---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
|
| HERC6 - HECT and RLD domain containing E3 ubiquitin protein ligase family member 6 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001165136.1 | Intron | NP_001158608.1 | ||||
| NM_017912.3 | Intron | NP_060382.3 | ||||
| XM_005263083.3 | Intron | XP_005263140.1 | ||||
| XM_011532053.2 | Intron | XP_011530355.1 | ||||
| XM_017008333.1 | Intron | XP_016863822.1 | ||||
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