Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GGACTGACCTTCAAGGATGTGGCTG[G/T]GGTCTTCACTGAGGAGGAGCTGGGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 604750 | ||||||||||||||||||||
Literature Links: |
ZNF234 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 |
ZNF234 - zinc finger protein 234 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001144824.1 | 462 | Missense Mutation | GGG,GTG | G,V 15 | NP_001138296.1 | |
NM_006630.2 | 462 | Missense Mutation | GGG,GTG | G,V 15 | NP_006621.1 | |
XM_006722974.3 | 462 | Missense Mutation | GGG,GTG | G,V 15 | XP_006723037.1 | |
XM_017026149.1 | 462 | Missense Mutation | GGG,GTG | G,V 15 | XP_016881638.1 | |
XM_017026150.1 | 462 | Missense Mutation | GGG,GTG | G,V 15 | XP_016881639.1 | |
XM_017026151.1 | 462 | Missense Mutation | GGG,GTG | G,V 15 | XP_016881640.1 | |
XM_017026152.1 | 462 | UTR 5 | XP_016881641.1 | |||
XM_017026153.1 | 462 | UTR 5 | XP_016881642.1 |