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- SNP ID:
- rs10426583
- Gene
-
MYDGFTNFAIP8L1 - Gene Name
- Set Membership:
- > HapMap
- Chromosome Location:
- Chr.19: 4650006 - 4650006 on Build GRCh38
- Polymorphism:
- C/T, Transition substitution
- Context Sequence [VIC/FAM]:
GGGTGGGAGTGGAGGCTGAGCAGGG[C/T]CTGGGGCAGTGAGAGAGACCGGGGG
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606746
MIM: 615869
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Literature Links: |
MYDGF PubMed Links | ||||||||||||||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
| 1000Genome | Applied Biosystems® | HapMap | ||||||
|---|---|---|---|---|---|---|---|---|
Global
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Caucasian - Not Available | CEPH (CEU)
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EAS
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African American - Not Available | YRI (Yoruba)
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SAS
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Chinese - Not Available | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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| MYDGF - myeloid derived growth factor | ||||||
|---|---|---|---|---|---|---|
| There are no transcripts associated with this gene. | ||||||
| TNFAIP8L1 - TNF alpha induced protein 8 like 1 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001167942.1 | Intron | NP_001161414.1 | ||||
| NM_152362.2 | Intron | NP_689575.2 | ||||
| XM_005259487.3 | Intron | XP_005259544.1 | ||||
| XM_011527680.2 | Intron | XP_011525982.1 | ||||
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