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Search Thermo Fisher Scientific
GAGGTATAACTGAAGCCTTTCCCAC[A/G]CACACCACACGTATAGGGCTTCTCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
ZNF229 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 |
ZNF229 - zinc finger protein 229 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001278510.2 | 2909 | Missense Mutation | CGT,TGT | R,C 795 | NP_001265439.2 | |
NM_014518.3 | 2909 | Missense Mutation | CGT,TGT | R,C 801 | NP_055333.3 | |
XM_006723372.3 | 2909 | Missense Mutation | CGT,TGT | R,C 773 | XP_006723435.1 | |
XM_011527292.1 | 2909 | Missense Mutation | CGT,TGT | R,C 795 | XP_011525594.1 | |
XM_017027280.1 | 2909 | Missense Mutation | CGT,TGT | R,C 455 | XP_016882769.1 |