Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GATGTAACAATTAAGGGATGAATGA[C/T]CCATGACTTTTTCTCCTCTCATACT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606697 | ||||||||||||||||||||
Literature Links: |
ZNF443 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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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 |
ZNF443 - zinc finger protein 443 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_005815.4 | 2110 | Missense Mutation | GAT,GGT | D,G 114 | NP_005806.2 | |
XM_011527622.2 | 2110 | Missense Mutation | GAT,GGT | D,G 82 | XP_011525924.1 | |
XM_011527623.2 | 2110 | Missense Mutation | GAT,GGT | D,G 161 | XP_011525925.2 | |
XM_017026139.1 | 2110 | Missense Mutation | GAT,GGT | D,G 161 | XP_016881628.1 | |
XM_017026140.1 | 2110 | Missense Mutation | GAT,GGT | D,G 116 | XP_016881629.1 |