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Search Thermo Fisher Scientific
TCCAGGCACACATAGGGTTTCTCAC[C/T]GGAGTGTGTCCTCTGGTGTCTGATG
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
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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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 | 1481 | Missense Mutation | AGT,GGT | S,G 377 | NP_001269424.1 | |
NM_001282496.1 | 1481 | Missense Mutation | AGT,GGT | S,G 377 | NP_001269425.1 | |
NM_001282497.1 | 1481 | Missense Mutation | AGT,GGT | S,G 418 | NP_001269426.1 | |
NM_001282498.1 | 1481 | Missense Mutation | AGT,GGT | S,G 287 | NP_001269427.1 | |
NM_001282499.1 | 1481 | Intron | NP_001269428.1 | |||
NM_001321800.1 | 1481 | Missense Mutation | AGT,GGT | S,G 377 | NP_001308729.1 | |
NM_001321801.1 | 1481 | Missense Mutation | AGT,GGT | S,G 418 | NP_001308730.1 | |
NM_001321802.1 | 1481 | Missense Mutation | AGT,GGT | S,G 417 | NP_001308731.1 | |
NM_001321803.1 | 1481 | Missense Mutation | AGT,GGT | S,G 417 | NP_001308732.1 | |
NM_001321805.1 | 1481 | Missense Mutation | AGT,GGT | S,G 376 | NP_001308734.1 | |
NM_024325.5 | 1481 | Missense Mutation | AGT,GGT | S,G 377 | NP_077301.4 | |
XM_017028062.1 | 1481 | Missense Mutation | AGT,GGT | S,G 377 | XP_016883551.1 |