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ATCTTCAACTCCATTTCCTGACAAA[C/T]GTGTTGTATTTGTTTTTTCTTTTCC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
ZNF280D 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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ZNF280D - zinc finger protein 280D | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001002843.2 | 2392 | Missense Mutation | ATT,GTT | I,V 832 | NP_001002843.1 | |
NM_001002844.2 | 2392 | Intron | NP_001002844.1 | |||
NM_001288588.1 | 2392 | Missense Mutation | ATT,GTT | I,V 845 | NP_001275517.1 | |
NM_001288589.1 | 2392 | Intron | NP_001275518.1 | |||
NM_017661.3 | 2392 | Missense Mutation | ATT,GTT | I,V 845 | NP_060131.2 | |
XM_005254481.3 | 2392 | Intron | XP_005254538.2 | |||
XM_005254483.3 | 2392 | Intron | XP_005254540.2 | |||
XM_005254484.3 | 2392 | Intron | XP_005254541.2 | |||
XM_005254485.3 | 2392 | Intron | XP_005254542.2 | |||
XM_011521701.1 | 2392 | Missense Mutation | ATT,GTT | I,V 780 | XP_011520003.1 | |
XM_011521702.1 | 2392 | Missense Mutation | ATT,GTT | I,V 845 | XP_011520004.1 | |
XM_011521704.2 | 2392 | Intron | XP_011520006.1 | |||
XM_011521707.2 | 2392 | Intron | XP_011520009.1 | |||
XM_011521708.1 | 2392 | Missense Mutation | ATT,GTT | I,V 739 | XP_011520010.1 | |
XM_011521709.1 | 2392 | Missense Mutation | ATT,GTT | I,V 739 | XP_011520011.1 | |
XM_011521710.1 | 2392 | Missense Mutation | ATT,GTT | I,V 739 | XP_011520012.1 | |
XM_011521711.1 | 2392 | Intron | XP_011520013.1 | |||
XM_017022344.1 | 2392 | Missense Mutation | ATT,GTT | I,V 845 | XP_016877833.1 | |
XM_017022345.1 | 2392 | Missense Mutation | ATT,GTT | I,V 845 | XP_016877834.1 | |
XM_017022346.1 | 2392 | Intron | XP_016877835.1 | |||
XM_017022347.1 | 2392 | Intron | XP_016877836.1 | |||
XM_017022348.1 | 2392 | Intron | XP_016877837.1 | |||
XM_017022349.1 | 2392 | Missense Mutation | ATT,GTT | I,V 357 | XP_016877838.1 |