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- SNP ID:
- rs202075563
- Gene
-
AGRNISG15 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.1: 1014092 - 1014092 on Build GRCh38
- Polymorphism:
- A/G, Transition substitution
- Context Sequence [VIC/FAM]:
GGCGCAGATCACCCAGAAGATCGGC[A/G]TGCACGCCTTCCAGCAGCGTCTGGC
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
5 submissions
|
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Phenotype: |
MIM: 103320
MIM: 147571
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Literature Links: |
AGRN 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
|
| AGRN - agrin | ||||||
|---|---|---|---|---|---|---|
| There are no transcripts associated with this gene. | ||||||
| ISG15 - ISG15 ubiquitin-like modifier | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_005101.3 | 219 | Missense Mutation | ATG,GTG | M,V 38 | NP_005092.1 | |
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