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AGAAGATGAAAAATTGAACATCCTG[C/T]CCAGCAAAAGGGACTTGGCGGCCGA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
2 submissions
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Phenotype: |
MIM: 608433 | ||||||||||||||||||||
Literature Links: |
LOC339529 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 |
LOC339529 - uncharacterized LOC339529 | ||||||
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There are no transcripts associated with this gene. |
ZBTB18 - zinc finger and BTB domain containing 18 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001278196.1 | 641 | Missense Mutation | CCC,TCC | P,S 171 | NP_001265125.1 | |
NM_006352.4 | 641 | Missense Mutation | CCC,TCC | P,S 171 | NP_006343.2 | |
NM_205768.2 | 641 | Missense Mutation | CCC,TCC | P,S 180 | NP_991331.1 | |
XM_005273006.2 | 641 | Missense Mutation | CCC,TCC | P,S 171 | XP_005273063.1 | |
XM_017000060.1 | 641 | Missense Mutation | CCC,TCC | P,S 171 | XP_016855549.1 |