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CCCCCGAGAGGCTTTAGAAGGGGCC[A/G]CCAGGCCTACACGTGGCAAGCGGAC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611712 MIM: 605725 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
HIPK4 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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HIPK4 - homeodomain interacting protein kinase 4 | ||||||
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There are no transcripts associated with this gene. |
PRX - periaxin | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_020956.2 | 5069 | UTR 3 | NP_066007.1 | |||
NM_181882.2 | 5069 | Missense Mutation | GCG,GTG | A,V 1384 | NP_870998.2 | |
XM_011527171.2 | 5069 | Missense Mutation | GCG,GTG | A,V 1384 | XP_011525473.1 | |
XM_017027046.1 | 5069 | Missense Mutation | GCG,GTG | A,V 1350 | XP_016882535.1 | |
XM_017027047.1 | 5069 | Missense Mutation | GCG,GTG | A,V 1350 | XP_016882536.1 |