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- SNP ID:
- rs202010328
- Gene
-
FGD5LOC152274 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.3: 14820164 - 14820164 on Build GRCh38
- Polymorphism:
- C/T, Transition substitution
- Context Sequence [VIC/FAM]:
TTTTTGCAGCGAGAGCTGTTCTCCT[C/T]TTTCTGAATCAGCGAAAGGTTTAGA
Genomic Map
Back To TopAssay Details
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 614788
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Literature Links: |
FGD5 PubMed Links | |||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
| 1000Genome | Applied Biosystems® | HapMap | |||
|---|---|---|---|---|---|
Global
|
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 |
| FGD5 - FYVE, RhoGEF and PH domain containing 5 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001320276.1 | 1203 | Missense Mutation | CTT,TTT | L,F 365 | NP_001307205.1 | |
| NM_152536.3 | 1203 | Missense Mutation | CTT,TTT | L,F 365 | NP_689749.3 | |
| XM_011533422.1 | 1203 | Missense Mutation | CTT,TTT | L,F 365 | XP_011531724.1 | |
| XM_011533423.1 | 1203 | Missense Mutation | CTT,TTT | L,F 365 | XP_011531725.1 | |
| LOC152274 - uncharacterized LOC152274 | ||||||
|---|---|---|---|---|---|---|
| There are no transcripts associated with this gene. | ||||||
Back To TopMore Information
Panther Classification:
Molecular Function -
G-protein modulator
protein-binding activity modulator
guanyl-nucleotide exchange factor
Gene Ontology Categories:
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