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ATCCGGACGCAGGGCCTTGAATACC[A/G]CACCCACAGGGCTGTGCTAGCTGCC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
5 submissions
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Phenotype: |
MIM: 607646 | ||||||||||||||||||||
Literature Links: |
DCST2 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 |
DCST2 - DC-STAMP domain containing 2 | ||||||
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There are no transcripts associated with this gene. |
ZBTB7B - zinc finger and BTB domain containing 7B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001252406.2 | 464 | Missense Mutation | CAC,CGC | H,R 80 | NP_001239335.1 | |
NM_001256455.1 | 464 | Missense Mutation | CAC,CGC | H,R 46 | NP_001243384.1 | |
XM_006711349.2 | 464 | Missense Mutation | CAC,CGC | H,R 46 | XP_006711412.2 | |
XM_006711353.1 | 464 | Missense Mutation | CAC,CGC | H,R 46 | XP_006711416.1 | |
XM_006711354.1 | 464 | Missense Mutation | CAC,CGC | H,R 46 | XP_006711417.1 | |
XM_006711356.3 | 464 | Missense Mutation | CAC,CGC | H,R 46 | XP_006711419.1 | |
XM_006711357.1 | 464 | Missense Mutation | CAC,CGC | H,R 46 | XP_006711420.1 | |
XM_006711358.1 | 464 | Missense Mutation | CAC,CGC | H,R 46 | XP_006711421.1 | |
XM_006711359.2 | 464 | Missense Mutation | CAC,CGC | H,R 46 | XP_006711422.1 | |
XM_011509598.2 | 464 | Missense Mutation | CAC,CGC | H,R 80 | XP_011507900.1 | |
XM_011509599.2 | 464 | Missense Mutation | CAC,CGC | H,R 46 | XP_011507901.1 | |
XM_017001399.1 | 464 | Missense Mutation | CAC,CGC | H,R 137 | XP_016856888.1 |