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TCTGTGATATCTTGCAAGTTTTGAA[C/T]TTTGGATAAAAGCCTCACCAAATTC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
ZNF841 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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ZNF841 - zinc finger protein 841 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001136499.1 | 4133 | Missense Mutation | AAT,AGT | N,S 693 | NP_001129971.1 | |
NM_001321349.1 | 4133 | Missense Mutation | AAT,AGT | N,S 577 | NP_001308278.1 | |
XM_011526833.2 | 4133 | Intron | XP_011525135.1 | |||
XM_017026652.1 | 4133 | Intron | XP_016882141.1 | |||
XM_017026653.1 | 4133 | Missense Mutation | AAT,AGT | N,S 694 | XP_016882142.1 | |
XM_017026654.1 | 4133 | Missense Mutation | AAT,AGT | N,S 694 | XP_016882143.1 | |
XM_017026655.1 | 4133 | Intron | XP_016882144.1 | |||
XM_017026656.1 | 4133 | Missense Mutation | AAT,AGT | N,S 693 | XP_016882145.1 | |
XM_017026657.1 | 4133 | Intron | XP_016882146.1 | |||
XM_017026658.1 | 4133 | Intron | XP_016882147.1 | |||
XM_017026659.1 | 4133 | Missense Mutation | AAT,AGT | N,S 695 | XP_016882148.1 | |
XM_017026660.1 | 4133 | Intron | XP_016882149.1 | |||
XM_017026661.1 | 4133 | Intron | XP_016882150.1 | |||
XM_017026662.1 | 4133 | Missense Mutation | AAT,AGT | N,S 693 | XP_016882151.1 | |
XM_017026663.1 | 4133 | Intron | XP_016882152.1 |