Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CTGCTGGCTTTCAGCCGCCTGTCTC[C/T]GCACACTTGATGCTGTTTCTATTTT
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 |
---|---|---|
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 |
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 | 427 | UTR 3 | NP_001007272.1 | |||
NM_001007272.1 | 427 | Intron | NP_001007273.1 | |||
NM_001007273.1 | 427 | Missense Mutation | AGA,GGA | R,G 68 | NP_001007274.1 | |
NM_001320842.1 | 427 | Missense Mutation | AGA,GGA | R,G 68 | NP_001307771.1 | |
NM_001320843.1 | 427 | UTR 5 | NP_001307772.1 | |||
NM_016364.3 | 427 | Intron | NP_057448.3 | |||
XM_005269883.3 | 427 | Missense Mutation | AGA,GGA | R,G 194 | XP_005269940.1 | |
XM_005269884.4 | 427 | Intron | XP_005269941.3 | |||
XM_005269887.1 | 427 | Missense Mutation | AGA,GGA | R,G 68 | XP_005269944.1 | |
XM_005269890.1 | 427 | Intron | XP_005269947.1 | |||
XM_011539853.1 | 427 | Missense Mutation | AGA,GGA | R,G 104 | XP_011538155.1 | |
XM_011539854.2 | 427 | UTR 5 | XP_011538156.1 | |||
XM_011539855.1 | 427 | Intron | XP_011538157.1 | |||
XM_011539856.2 | 427 | UTR 5 | XP_011538158.1 | |||
XM_017016313.1 | 427 | Intron | XP_016871802.1 | |||
XM_017016314.1 | 427 | Missense Mutation | AGA,GGA | R,G 194 | XP_016871803.1 |
SAMD8 - sterile alpha motif domain containing 8 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001174156.1 | 427 | Intron | NP_001167627.1 | |||
NM_144660.2 | 427 | Intron | NP_653261.1 | |||
XM_005269541.4 | 427 | Intron | XP_005269598.1 | |||
XM_011539311.1 | 427 | Intron | XP_011537613.1 | |||
XM_011539312.2 | 427 | Intron | XP_011537614.1 | |||
XM_017015738.1 | 427 | Intron | XP_016871227.1 | |||
XM_017015739.1 | 427 | Intron | XP_016871228.1 |