Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
ACGCCGTGCAGAAGCCACAGGCCTC[A/G]TCTGGCACCCACTCCGGGGGGTCTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 614176 | ||||||||||||||||||||
Literature Links: |
MXD4 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 |
MXD4 - MAX dimerization protein 4 | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |
ZFYVE28 - zinc finger FYVE-type containing 28 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001172656.1 | 2825 | Silent Mutation | GAC,GAT | D,D 787 | NP_001166127.1 | |
NM_001172657.1 | 2825 | Intron | NP_001166128.1 | |||
NM_001172658.1 | 2825 | Intron | NP_001166129.1 | |||
NM_001172659.1 | 2825 | Silent Mutation | GAC,GAT | D,D 747 | NP_001166130.1 | |
NM_001172660.1 | 2825 | Intron | NP_001166131.1 | |||
NM_020972.2 | 2825 | Silent Mutation | GAC,GAT | D,D 817 | NP_066023.2 | |
XM_006713900.3 | 2825 | Silent Mutation | GAC,GAT | D,D 817 | XP_006713963.1 | |
XM_006713902.3 | 2825 | Missense Mutation | ACG,ATG | T,M 891 | XP_006713965.1 | |
XM_006713904.3 | 2825 | Intron | XP_006713967.1 | |||
XM_011513540.2 | 2825 | Silent Mutation | GAC,GAT | D,D 703 | XP_011511842.1 | |
XM_011513541.2 | 2825 | Intron | XP_011511843.1 | |||
XM_017008502.1 | 2825 | Silent Mutation | GAC,GAT | D,D 759 | XP_016863991.1 | |
XM_017008503.1 | 2825 | Missense Mutation | ACG,ATG | T,M 892 | XP_016863992.1 | |
XM_017008504.1 | 2825 | Missense Mutation | ACG,ATG | T,M 892 | XP_016863993.1 | |
XM_017008505.1 | 2825 | Silent Mutation | GAC,GAT | D,D 703 | XP_016863994.1 | |
XM_017008506.1 | 2825 | Intron | XP_016863995.1 | |||
XM_017008507.1 | 2825 | Intron | XP_016863996.1 | |||
XM_017008508.1 | 2825 | Intron | XP_016863997.1 | |||
XM_017008509.1 | 2825 | Intron | XP_016863998.1 | |||
XM_017008510.1 | 2825 | Intron | XP_016863999.1 |