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CCTGCTCCAAGGCTGGCCCATGCTC[A/G]CAGTACTCTGCTCGAACCCGGAGCC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 164176 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
DEDD2 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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DEDD2 - death effector domain containing 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001270614.1 | 766 | Silent Mutation | TGC,TGT | C,C 207 | NP_001257543.1 | |
NM_001270615.1 | 766 | Silent Mutation | TGC,TGT | C,C 202 | NP_001257544.1 | |
NM_133328.3 | 766 | Silent Mutation | TGC,TGT | C,C 207 | NP_579874.1 | |
XM_011526569.1 | 766 | Silent Mutation | TGC,TGT | C,C 247 | XP_011524871.1 | |
XM_011526571.1 | 766 | Missense Mutation | GCG,GTG | A,V 240 | XP_011524873.1 | |
XM_011526572.1 | 766 | Nonsense Mutation | CGA,TGA | R,* 215 | XP_011524874.1 | |
XM_017026402.1 | 766 | Silent Mutation | TGC,TGT | C,C 247 | XP_016881891.1 | |
XM_017026403.1 | 766 | Missense Mutation | GCG,GTG | A,V 268 | XP_016881892.1 |
POU2F2 - POU class 2 homeobox 2 | ||||||
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There are no transcripts associated with this gene. |