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- SNP ID:
- rs149527990
- Gene
-
MPNDSH3GL1 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.19: 4362350 - 4362350 on Build GRCh38
- Polymorphism:
- A/G, Transition substitution
- Context Sequence [VIC/FAM]:
TCACGCATGCTCCGGCTAGGGGTCC[A/G]GATGGGCTTGTCGGAAGATCGGAAA
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 601768
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Literature Links: |
MPND 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 |
| MPND - MPN domain containing | ||||||
|---|---|---|---|---|---|---|
| There are no transcripts associated with this gene. | ||||||
| SH3GL1 - SH3 domain containing GRB2 like 1, endophilin A2 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001199943.1 | Intron | NP_001186872.1 | ||||
| NM_001199944.1 | Intron | NP_001186873.1 | ||||
| NM_003025.3 | Intron | NP_003016.1 | ||||
| XM_011528183.2 | Intron | XP_011526485.1 | ||||
| XM_017027146.1 | Intron | XP_016882635.1 | ||||
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