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- SNP ID:
- rs73007706
- Gene
-
LSM4 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.19: 18311852 - 18311852 on Build GRCh38
- Polymorphism:
- G/T, Transversion substitution
- Context Sequence [VIC/FAM]:
TTCAGGAAGAAGCGCCTCCCCCCTC[G/T]AGCCCTGTTGTCCTGTCAAGGTGAC
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607284
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Literature Links: |
LSM4 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
|
| LSM4 - LSM4 homolog, U6 small nuclear RNA and mRNA degradation associated | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001252129.1 | Intron | NP_001239058.1 | ||||
| NM_012321.4 | Intron | NP_036453.1 | ||||
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