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- SNP ID:
- rs778502580
- Gene
-
POMGNT2 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.3: 43079465 - 43079465 on Build GRCh38
- Polymorphism:
- C/A, Transversion substitution
- Context Sequence [VIC/FAM]:
CTTCCTCCTCCCTGCTAAGGAACTT[C/A]TCCAGGGGTACAAATGTTCAGGATG
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 614828
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Literature Links: |
POMGNT2 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 |
| POMGNT2 - protein O-linked mannose N-acetylglucosaminyltransferase 2 (beta 1,4-) | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_032806.5 | 2320 | UTR 3 | NP_116195.2 | |||
| XM_005265515.2 | 2320 | UTR 3 | XP_005265572.1 | |||
| XM_011534163.2 | 2320 | UTR 3 | XP_011532465.1 | |||
| XM_011534164.1 | 2320 | UTR 3 | XP_011532466.1 | |||
| XM_017007353.1 | 2320 | UTR 3 | XP_016862842.1 | |||
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