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GTTGATGGAGCCTGAATTATGTGTC[C/T]GTACACTAGCTGCAAATGAAGCTGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
4 submissions
|
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Phenotype: |
MIM: 610964 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SMG7 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
|
SMG7 - SMG7, nonsense mediated mRNA decay factor | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001174061.1 | Intron | NP_001167532.1 | ||||
NM_173156.2 | Intron | NP_775179.1 | ||||
NM_201568.2 | Intron | NP_963862.1 | ||||
NM_201569.2 | Intron | NP_963863.2 | ||||
XM_005245648.3 | Intron | XP_005245705.1 | ||||
XM_005245649.3 | Intron | XP_005245706.1 | ||||
XM_005245652.3 | Intron | XP_005245709.1 | ||||
XM_005245653.4 | Intron | XP_005245710.1 | ||||
XM_006711676.3 | Intron | XP_006711739.1 | ||||
XM_006711678.3 | Intron | XP_006711741.1 | ||||
XM_011510205.2 | Intron | XP_011508507.1 | ||||
XM_011510206.2 | Intron | XP_011508508.1 | ||||
XM_011510207.2 | Intron | XP_011508509.1 | ||||
XM_011510208.2 | Intron | XP_011508510.1 | ||||
XM_011510209.2 | Intron | XP_011508511.1 | ||||
XM_011510210.2 | Intron | XP_011508512.1 | ||||
XM_017002966.1 | Intron | XP_016858455.1 | ||||
XM_017002967.1 | Intron | XP_016858456.1 | ||||
XM_017002968.1 | Intron | XP_016858457.1 | ||||
XM_017002969.1 | Intron | XP_016858458.1 | ||||
XM_017002970.1 | Intron | XP_016858459.1 | ||||
XM_017002971.1 | Intron | XP_016858460.1 |