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ATGGTGTGAGAAGCTTGAGTGATAG[A/C]TAAAGGCCTTCCCACATTCCCGACA
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 - Not Available | Caucasian - Not Available | CEPH (CEU)
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EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS - Not Available | Chinese - Not Available | JPT (Japanese)
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AFR - Not Available | Japanese - Not Available | CHB (Han Chinese)
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EUR - Not Available | |||||
AMR - Not Available |
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 | 1391 | Missense Mutation | AGC,ATC | S,I 372 | NP_001284552.1 | |
NM_001322821.1 | 1391 | Missense Mutation | AGC,ATC | S,I 389 | NP_001309750.1 | |
NM_001322823.1 | 1391 | Missense Mutation | AGC,ATC | S,I 364 | NP_001309752.1 | |
NM_001322825.1 | 1391 | Missense Mutation | AGC,ATC | S,I 364 | NP_001309754.1 | |
NM_001322826.1 | 1391 | Missense Mutation | AGC,ATC | S,I 341 | NP_001309755.1 | |
NM_001322827.1 | 1391 | Missense Mutation | AGC,ATC | S,I 341 | NP_001309756.1 | |
NM_001322828.1 | 1391 | Missense Mutation | AGC,ATC | S,I 307 | NP_001309757.1 | |
NM_153257.4 | 1391 | Missense Mutation | AGC,ATC | S,I 395 | NP_694989.2 | |
XM_011527486.2 | 1391 | Missense Mutation | AGC,ATC | S,I 268 | XP_011525788.1 | |
XM_017027470.1 | 1391 | Missense Mutation | AGC,ATC | S,I 351 | XP_016882959.1 |
Set Membership: |
HapMap |