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- SNP ID:
- rs377628364
- Gene
-
ACTG1FSCN2 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.17: 81511192 - 81511192 on Build GRCh38
- Polymorphism:
- G/A, Transition substitution
- Context Sequence [VIC/FAM]:
CCTTTAGCTCACAACACCTACCCAG[G/A]AAGGAAGGCTGGAACAGCGCCTCCG
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 102560
MIM: 607643
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Literature Links: |
ACTG1 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 |
| ACTG1 - actin gamma 1 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001199954.1 | 937 | Silent Mutation | TTC,TTT | F,F 266 | NP_001186883.1 | |
| NM_001614.3 | 937 | Silent Mutation | TTC,TTT | F,F 266 | NP_001605.1 | |
| FSCN2 - fascin actin-bundling protein 2, retinal | ||||||
|---|---|---|---|---|---|---|
| There are no transcripts associated with this gene. | ||||||
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