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Search Thermo Fisher Scientific
CTTCCCACATTCGTTACATTCATAG[C/T]GTTTTTCACCATTATGAATTCTTAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608640 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ZNF461 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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ZNF461 - zinc finger protein 461 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001297623.2 | 1022 | Missense Mutation | CAC,CGC | H,R 249 | NP_001284552.1 | |
NM_001322821.1 | 1022 | Missense Mutation | CAC,CGC | H,R 266 | NP_001309750.1 | |
NM_001322823.1 | 1022 | Missense Mutation | CAC,CGC | H,R 241 | NP_001309752.1 | |
NM_001322825.1 | 1022 | Missense Mutation | CAC,CGC | H,R 241 | NP_001309754.1 | |
NM_001322826.1 | 1022 | Missense Mutation | CAC,CGC | H,R 218 | NP_001309755.1 | |
NM_001322827.1 | 1022 | Missense Mutation | CAC,CGC | H,R 218 | NP_001309756.1 | |
NM_001322828.1 | 1022 | Missense Mutation | CAC,CGC | H,R 184 | NP_001309757.1 | |
NM_153257.4 | 1022 | Missense Mutation | CAC,CGC | H,R 272 | NP_694989.2 | |
XM_011527486.2 | 1022 | Missense Mutation | CAC,CGC | H,R 145 | XP_011525788.1 | |
XM_017027470.1 | 1022 | Missense Mutation | CAC,CGC | H,R 228 | XP_016882959.1 |