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TTATGCACTGGGGATCCGAGTGTCC[A/G]GGAGCTCCGGCTTGGCATCCACTGT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607382 MIM: 612536 | ||||||||||||||||||||
Literature Links: |
CLIP3 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
CLIP3 - CAP-Gly domain containing linker protein 3 | ||||||
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There are no transcripts associated with this gene. |
LOC101927572 - uncharacterized LOC101927572 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001290056.1 | 1154 | Intron | NP_001276985.1 |
THAP8 - THAP domain containing 8 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_152658.2 | 1154 | Missense Mutation | CCG,CTG | P,L 267 | NP_689871.1 | |
XM_005258623.2 | 1154 | Missense Mutation | CCG,CTG | P,L 224 | XP_005258680.1 | |
XM_011526604.2 | 1154 | Missense Mutation | CCG,CTG | P,L 224 | XP_011524906.1 |