Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AGGCTTCTCCCCTGAGTGTATCCTC[C/T]GGTGTTTTCTGAGGGTTGACTTATC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
ZNF343 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
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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 |
ZNF343 - zinc finger protein 343 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001282495.1 | 1551 | Missense Mutation | CAG,CGG | Q,R 400 | NP_001269424.1 | |
NM_001282496.1 | 1551 | Missense Mutation | CAG,CGG | Q,R 400 | NP_001269425.1 | |
NM_001282497.1 | 1551 | Missense Mutation | CAG,CGG | Q,R 441 | NP_001269426.1 | |
NM_001282498.1 | 1551 | Missense Mutation | CAG,CGG | Q,R 310 | NP_001269427.1 | |
NM_001282499.1 | 1551 | Intron | NP_001269428.1 | |||
NM_001321800.1 | 1551 | Missense Mutation | CAG,CGG | Q,R 400 | NP_001308729.1 | |
NM_001321801.1 | 1551 | Missense Mutation | CAG,CGG | Q,R 441 | NP_001308730.1 | |
NM_001321802.1 | 1551 | Missense Mutation | CAG,CGG | Q,R 440 | NP_001308731.1 | |
NM_001321803.1 | 1551 | Missense Mutation | CAG,CGG | Q,R 440 | NP_001308732.1 | |
NM_001321805.1 | 1551 | Missense Mutation | CAG,CGG | Q,R 399 | NP_001308734.1 | |
NM_024325.5 | 1551 | Missense Mutation | CAG,CGG | Q,R 400 | NP_077301.4 | |
XM_017028062.1 | 1551 | Missense Mutation | CAG,CGG | Q,R 400 | XP_016883551.1 |