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- SNP ID:
- rs73637004
- Gene
-
DCX - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.X: 111310709 - 111310709 on Build GRCh38
- Polymorphism:
- C/T, Transition substitution
- Context Sequence [VIC/FAM]:
GAGTAATTTTAAAAATAAAATGAAA[C/T]ACTGAAAATTCCACAGTTAAGAAAA
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 300121
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Literature Links: |
DCX 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
|
| DCX - doublecortin | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_000555.3 | Intron | NP_000546.2 | ||||
| NM_001195553.1 | Intron | NP_001182482.1 | ||||
| NM_178151.2 | Intron | NP_835364.1 | ||||
| NM_178152.2 | Intron | NP_835365.1 | ||||
| NM_178153.2 | Intron | NP_835366.1 | ||||
| XM_011530878.2 | Intron | XP_011529180.1 | ||||
| XM_011530879.2 | Intron | XP_011529181.1 | ||||
| XM_011530880.2 | Intron | XP_011529182.1 | ||||
| XM_017029312.1 | Intron | XP_016884801.1 | ||||
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