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- SNP ID:
- rs770806535
- Gene
-
MYOT - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.5: 137877915 - 137877915 on Build GRCh38
- Polymorphism:
- G/A, Transition substitution
- Context Sequence [VIC/FAM]:
TCAGTTAGACCTAGGACTCTCTATG[G/A]TGTCTACACGGACAGGGAATATATG
Genomic Map
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Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604103
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Literature Links: |
MYOT 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 |
| MYOT - myotilin | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001135940.1 | Intron | NP_001129412.1 | ||||
| NM_001300911.1 | Intron | NP_001287840.1 | ||||
| NM_006790.2 | Intron | NP_006781.1 | ||||
| XM_017010060.1 | Intron | XP_016865549.1 | ||||
| XM_017010061.1 | Intron | XP_016865550.1 | ||||
| XM_017010062.1 | Intron | XP_016865551.1 | ||||
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