Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GGAAGTGATGCTGTATTTTCAAAAC[C/T]GATTTTCAATCCTTCGTCGGTAGCC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 615254 | ||||||||||||||||||||
Literature Links: |
ZBED9 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 |
ZBED9 - zinc finger BED-type containing 9 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_052923.1 | 3729 | Missense Mutation | AGT,GGT | S,G 1239 | NP_443155.1 | |
XM_011514283.2 | 3729 | Missense Mutation | AGT,GGT | S,G 1088 | XP_011512585.1 | |
XM_011514284.2 | 3729 | Missense Mutation | AGT,GGT | S,G 1088 | XP_011512586.1 | |
XM_011514285.2 | 3729 | Missense Mutation | AGT,GGT | S,G 1088 | XP_011512587.1 | |
XM_011514286.2 | 3729 | Missense Mutation | AGT,GGT | S,G 1088 | XP_011512588.1 | |
XM_011514287.2 | 3729 | Missense Mutation | AGT,GGT | S,G 1088 | XP_011512589.1 | |
XM_011514288.2 | 3729 | Missense Mutation | AGT,GGT | S,G 1043 | XP_011512590.1 | |
XM_017010231.1 | 3729 | Missense Mutation | AGT,GGT | S,G 1088 | XP_016865720.1 |