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- SNP ID:
- rs11673223
- Gene
-
C19orf38DNM2MIR6793TMED1 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.19: 10838431 - 10838431 on Build GRCh38
- Polymorphism:
- A/C, Transversion substitution
- Context Sequence [VIC/FAM]:
TGTCAAAAAGAAAATAAAAATAACC[A/C]TTTTAAAATTAACAATTCAGTGGCA
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 602378
MIM: 605395
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Literature Links: |
C19orf38 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
|
| C19orf38 - chromosome 19 open reading frame 38 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001136482.1 | Intron | NP_001129954.1 | ||||
| XM_005259846.4 | Intron | XP_005259903.1 | ||||
| XM_005259847.4 | Intron | XP_005259904.1 | ||||
| DNM2 - dynamin 2 | ||||||
|---|---|---|---|---|---|---|
| There are no transcripts associated with this gene. | ||||||
| MIR6793 - microRNA 6793 | ||||||
|---|---|---|---|---|---|---|
| There are no transcripts associated with this gene. | ||||||
| TMED1 - transmembrane p24 trafficking protein 1 | ||||||
|---|---|---|---|---|---|---|
| There are no transcripts associated with this gene. | ||||||
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