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GCGCGGAGGACACAGCCGCAGGGGC[C/T]GCGGGACCTTGGCGCTTGAGCATGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606199 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CTD-2194D22.4 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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CTD-2194D22.4 - uncharacterized LOC101929081 | ||||||
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There are no transcripts associated with this gene. |
IRX4 - iroquois homeobox 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001278632.1 | 1421 | Silent Mutation | GCA,GCG | A,A 401 | NP_001265561.1 | |
NM_001278633.1 | 1421 | Silent Mutation | GCA,GCG | A,A 427 | NP_001265562.1 | |
NM_001278634.1 | 1421 | Silent Mutation | GCA,GCG | A,A 401 | NP_001265563.1 | |
NM_001278635.1 | 1421 | Silent Mutation | GCA,GCG | A,A 427 | NP_001265564.1 | |
NM_016358.2 | 1421 | Silent Mutation | GCA,GCG | A,A 401 | NP_057442.1 |