Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TGAAACTTAAAATGACTAATTTCAA[C/T]TTCTTTCTTTTTCGTCTTCCAGGTC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
|||||||||||||||||||||
Literature Links: |
ZNF280D PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||
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 |
ZNF280D - zinc finger protein 280D | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001002843.2 | 2795 | Missense Mutation | AAT,AGT | N,S 966 | NP_001002843.1 | |
NM_001002844.2 | 2795 | Intron | NP_001002844.1 | |||
NM_001288588.1 | 2795 | Missense Mutation | AAT,AGT | N,S 979 | NP_001275517.1 | |
NM_001288589.1 | 2795 | Intron | NP_001275518.1 | |||
NM_017661.3 | 2795 | Missense Mutation | AAT,AGT | N,S 979 | NP_060131.2 | |
XM_005254481.3 | 2795 | Intron | XP_005254538.2 | |||
XM_005254483.3 | 2795 | Intron | XP_005254540.2 | |||
XM_005254484.3 | 2795 | Intron | XP_005254541.2 | |||
XM_005254485.3 | 2795 | Intron | XP_005254542.2 | |||
XM_011521701.1 | 2795 | Missense Mutation | AAT,AGT | N,S 914 | XP_011520003.1 | |
XM_011521702.1 | 2795 | Missense Mutation | AAT,AGT | N,S 979 | XP_011520004.1 | |
XM_011521704.2 | 2795 | Intron | XP_011520006.1 | |||
XM_011521707.2 | 2795 | Intron | XP_011520009.1 | |||
XM_011521708.1 | 2795 | Missense Mutation | AAT,AGT | N,S 873 | XP_011520010.1 | |
XM_011521709.1 | 2795 | Missense Mutation | AAT,AGT | N,S 873 | XP_011520011.1 | |
XM_011521710.1 | 2795 | Missense Mutation | AAT,AGT | N,S 873 | XP_011520012.1 | |
XM_011521711.1 | 2795 | Intron | XP_011520013.1 | |||
XM_017022344.1 | 2795 | Missense Mutation | AAT,AGT | N,S 979 | XP_016877833.1 | |
XM_017022345.1 | 2795 | Missense Mutation | AAT,AGT | N,S 979 | XP_016877834.1 | |
XM_017022346.1 | 2795 | Intron | XP_016877835.1 | |||
XM_017022347.1 | 2795 | Intron | XP_016877836.1 | |||
XM_017022348.1 | 2795 | Intron | XP_016877837.1 | |||
XM_017022349.1 | 2795 | Missense Mutation | AAT,AGT | N,S 491 | XP_016877838.1 |