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ACCTCAGCAAGGTTATATTCCTCCA[A/G]TGGCACAGCCAGGACTGCCACCAGT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603428 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ZNF207 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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ZNF207 - zinc finger protein 207 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001032293.2 | 704 | Intron | NP_001027464.1 | |||
NM_001098507.1 | 704 | Intron | NP_001091977.1 | |||
NM_003457.3 | 704 | Intron | NP_003448.1 | |||
XM_011525185.2 | 704 | Missense Mutation | ATG,GTG | M,V 88 | XP_011523487.1 | |
XM_017025019.1 | 704 | Missense Mutation | ATG,GTG | M,V 142 | XP_016880508.1 | |
XM_017025020.1 | 704 | Intron | XP_016880509.1 |