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CCTAAAGCCTGGGGTTATGGGGTGT[C/G]TATGCAGTGAGCCCTTCCATGCACT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
LOC101928464 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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LOC101928464 - uncharacterized LOC101928464 | ||||||
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There are no transcripts associated with this gene. |
ZNF433 - zinc finger protein 433 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001080411.2 | 2251 | Missense Mutation | CAC,GAC | H,D 671 | NP_001073880.1 | |
NM_001308346.1 | 2251 | Missense Mutation | CAC,GAC | H,D 670 | NP_001295275.1 | |
NM_001308348.1 | 2251 | Missense Mutation | CAC,GAC | H,D 668 | NP_001295277.1 | |
NM_001308351.1 | 2251 | Missense Mutation | CAC,GAC | H,D 636 | NP_001295280.1 | |
NM_001308355.1 | 2251 | Missense Mutation | CAC,GAC | H,D 636 | NP_001295284.1 | |
NM_001308357.1 | 2251 | Missense Mutation | CAC,GAC | H,D 636 | NP_001295286.1 | |
XM_006722661.3 | 2251 | Missense Mutation | CAC,GAC | H,D 636 | XP_006722724.1 | |
XM_011527725.2 | 2251 | Missense Mutation | CAC,GAC | H,D 682 | XP_011526027.1 | |
XM_011527728.2 | 2251 | Missense Mutation | CAC,GAC | H,D 670 | XP_011526030.1 | |
XM_011527729.2 | 2251 | Missense Mutation | CAC,GAC | H,D 670 | XP_011526031.1 | |
XM_017026413.1 | 2251 | Intron | XP_016881902.1 |