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GAGGTCGAAGAAGGGGTTGTCGTCC[A/G]CCTCGATGCCATAGTACTCCAGGGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 613191 MIM: 611575 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
DUSP13 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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DUSP13 - dual specificity phosphatase 13 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001007271.1 | 815 | UTR 3 | NP_001007272.1 | |||
NM_001007272.1 | 815 | Missense Mutation | GCG,GTG | A,V 154 | NP_001007273.1 | |
NM_001007273.1 | 815 | Missense Mutation | GCG,GTG | A,V 197 | NP_001007274.1 | |
NM_001320842.1 | 815 | Missense Mutation | GCG,GTG | A,V 197 | NP_001307771.1 | |
NM_001320843.1 | 815 | Missense Mutation | GCG,GTG | A,V 104 | NP_001307772.1 | |
NM_016364.3 | 815 | Missense Mutation | GCG,GTG | A,V 104 | NP_057448.3 | |
XM_005269883.3 | 815 | Missense Mutation | GCG,GTG | A,V 323 | XP_005269940.1 | |
XM_005269884.4 | 815 | Missense Mutation | GCG,GTG | A,V 240 | XP_005269941.3 | |
XM_005269887.1 | 815 | Missense Mutation | GCG,GTG | A,V 197 | XP_005269944.1 | |
XM_005269890.1 | 815 | Missense Mutation | GCG,GTG | A,V 104 | XP_005269947.1 | |
XM_011539853.1 | 815 | Missense Mutation | GCG,GTG | A,V 233 | XP_011538155.1 | |
XM_011539854.2 | 815 | Missense Mutation | GCG,GTG | A,V 104 | XP_011538156.1 | |
XM_011539855.1 | 815 | Missense Mutation | GCG,GTG | A,V 104 | XP_011538157.1 | |
XM_011539856.2 | 815 | Missense Mutation | GCG,GTG | A,V 104 | XP_011538158.1 | |
XM_017016313.1 | 815 | Missense Mutation | GCG,GTG | A,V 152 | XP_016871802.1 | |
XM_017016314.1 | 815 | Intron | XP_016871803.1 |
SAMD8 - sterile alpha motif domain containing 8 | ||||||
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There are no transcripts associated with this gene. |