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- SNP ID:
- rs139801882
- Gene
-
C19orf45PEX11G - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.19: 7501183 - 7501183 on Build GRCh38
- Polymorphism:
- A/G, Transition substitution
- Context Sequence [VIC/FAM]:
CCTGCACCTGCACGAGGACGCGCAC[A/G]CCGGGATCGGCCTCTCCAACGCGCA
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607583
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Literature Links: |
C19orf45 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
|
| C19orf45 - chromosome 19 open reading frame 45 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_198534.2 | 502 | Missense Mutation | ACC,GCC | T,A 121 | NP_940936.2 | |
| XM_005272473.3 | 502 | Missense Mutation | ACC,GCC | T,A 121 | XP_005272530.1 | |
| XM_011527993.1 | 502 | Missense Mutation | ACC,GCC | T,A 121 | XP_011526295.1 | |
| XM_011527995.2 | 502 | Missense Mutation | ACC,GCC | T,A 121 | XP_011526297.1 | |
| PEX11G - peroxisomal biogenesis factor 11 gamma | ||||||
|---|---|---|---|---|---|---|
| There are no transcripts associated with this gene. | ||||||
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