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AGAAAAGCCTCCTGGGGGAAAGGGT[A/G]TCCTTCAGTTCCATGATTTAAACTT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 125660 MIM: 615950 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
DES 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
|
DES - desmin | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |
SPEG - SPEG complex locus | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001173476.1 | Intron | NP_001166947.1 | ||||
NM_005876.4 | Intron | NP_005867.3 | ||||
XM_005246237.2 | Intron | XP_005246294.1 | ||||
XM_005246239.2 | Intron | XP_005246296.1 | ||||
XM_005246240.2 | Intron | XP_005246297.1 | ||||
XM_005246241.1 | Intron | XP_005246298.1 | ||||
XM_005246242.4 | Intron | XP_005246299.1 | ||||
XM_006712189.3 | Intron | XP_006712252.1 | ||||
XM_006712193.3 | Intron | XP_006712256.1 | ||||
XM_011510479.2 | Intron | XP_011508781.1 | ||||
XM_011510483.2 | Intron | XP_011508785.2 | ||||
XM_017003157.1 | Intron | XP_016858646.1 | ||||
XM_017003158.1 | Intron | XP_016858647.1 | ||||
XM_017003159.1 | Intron | XP_016858648.1 | ||||
XM_017003160.1 | Intron | XP_016858649.1 | ||||
XM_017003161.1 | Intron | XP_016858650.1 | ||||
XM_017003162.1 | Intron | XP_016858651.1 |