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TCTTCACTGAGGAGGAGCTGGGGCT[G/T]CTGGACCCTGTCCAGAGGAATCTGT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604750 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ZNF234 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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ZNF234 - zinc finger protein 234 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001144824.1 | 490 | Silent Mutation | CTG,CTT | L,L 24 | NP_001138296.1 | |
NM_006630.2 | 490 | Silent Mutation | CTG,CTT | L,L 24 | NP_006621.1 | |
XM_006722974.3 | 490 | Silent Mutation | CTG,CTT | L,L 24 | XP_006723037.1 | |
XM_017026149.1 | 490 | Silent Mutation | CTG,CTT | L,L 24 | XP_016881638.1 | |
XM_017026150.1 | 490 | Silent Mutation | CTG,CTT | L,L 24 | XP_016881639.1 | |
XM_017026151.1 | 490 | Silent Mutation | CTG,CTT | L,L 24 | XP_016881640.1 | |
XM_017026152.1 | 490 | UTR 5 | XP_016881641.1 | |||
XM_017026153.1 | 490 | UTR 5 | XP_016881642.1 |