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CCCCAGCCAATCTAGTTTCACAGGT[C/T]TTTTGAAGAGAATGGAACAAAGAGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 615708 | ||||||||||||||||||||
Literature Links: |
ZNF451 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 |
ZNF451 - zinc finger protein 451 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001031623.2 | 782 | Intron | NP_001026794.1 | |||
NM_001257273.1 | 782 | Missense Mutation | CTT,TTT | L,F 261 | NP_001244202.1 | |
NM_015555.2 | 782 | Intron | NP_056370.2 | |||
XM_005248994.1 | 782 | Intron | XP_005249051.1 | |||
XM_011514460.1 | 782 | Intron | XP_011512762.1 | |||
XM_011514461.1 | 782 | Intron | XP_011512763.1 | |||
XM_011514462.2 | 782 | Intron | XP_011512764.1 | |||
XM_011514463.2 | 782 | Missense Mutation | CTT,TTT | L,F 233 | XP_011512765.1 |