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- SNP ID:
- rs41278106
- Gene
-
CHD6 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.20: 41403669 - 41403669 on Build GRCh38
- Polymorphism:
- A/G, Transition substitution
- Context Sequence [VIC/FAM]:
GGCTCCAGAAAGAACCTTATTCTTG[A/G]TGAAGGAAAGCCTGAAGTGAAAATC
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 616114
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Literature Links: |
CHD6 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
|
| CHD6 - chromodomain helicase DNA binding protein 6 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_032221.4 | 8705 | UTR 3 | NP_115597.3 | |||
| XM_005260573.2 | 8705 | UTR 3 | XP_005260630.1 | |||
| XM_005260576.4 | 8705 | UTR 3 | XP_005260633.1 | |||
| XM_011529080.2 | 8705 | UTR 3 | XP_011527382.1 | |||
| XM_011529082.2 | 8705 | UTR 3 | XP_011527384.1 | |||
| XM_017028099.1 | 8705 | UTR 3 | XP_016883588.1 | |||
| XM_017028100.1 | 8705 | UTR 3 | XP_016883589.1 | |||
| XM_017028101.1 | 8705 | UTR 3 | XP_016883590.1 | |||
| XM_017028102.1 | 8705 | Intron | XP_016883591.1 | |||
| XM_017028103.1 | 8705 | UTR 3 | XP_016883592.1 | |||
| XM_017028104.1 | 8705 | Intron | XP_016883593.1 | |||
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