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- SNP ID:
- rs147804735
- Gene
-
AMELXARHGAP6 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.X: 11297153 - 11297153 on Build GRCh38
- Polymorphism:
- C/T, Transition substitution
- Context Sequence [VIC/FAM]:
CTTGGTTCTAACCCAGCTAGTAAAA[C/T]GTAAGGATTAGGTAAGATGTTATTT
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 300391
MIM: 300118
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Literature Links: |
AMELX 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
|
| AMELX - amelogenin, X-linked | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001142.2 | Intron | NP_001133.1 | ||||
| NM_182680.1 | Intron | NP_872621.1 | ||||
| NM_182681.1 | Intron | NP_872622.1 | ||||
| XM_017029404.1 | Intron | XP_016884893.1 | ||||
| ARHGAP6 - Rho GTPase activating protein 6 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001287242.1 | Intron | NP_001274171.1 | ||||
| NM_006125.2 | Intron | NP_006116.2 | ||||
| NM_013423.2 | Intron | NP_038267.1 | ||||
| NM_013427.2 | Intron | NP_038286.2 | ||||
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