Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TGTTGAGCAGGTCCGGATCCTCCGC[A/G]GGCTGGGGGCCATCCAGCCCGGGGT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 300608 | ||||||||||||||||||||
Literature Links: |
DACH2 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 |
DACH2 - dachshund family transcription factor 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001139514.1 | 566 | Missense Mutation | AGG,GGG | R,G 133 | NP_001132986.1 | |
NM_001139515.1 | 566 | Intron | NP_001132987.1 | |||
NM_053281.3 | 566 | Missense Mutation | AGG,GGG | R,G 133 | NP_444511.1 | |
XM_011530846.2 | 566 | Missense Mutation | AGG,GGG | R,G 133 | XP_011529148.1 | |
XM_011530847.2 | 566 | Missense Mutation | AGG,GGG | R,G 133 | XP_011529149.1 | |
XM_011530848.2 | 566 | Missense Mutation | AGG,GGG | R,G 133 | XP_011529150.1 | |
XM_017029254.1 | 566 | Missense Mutation | AGG,GGG | R,G 133 | XP_016884743.1 | |
XM_017029255.1 | 566 | Missense Mutation | AGG,GGG | R,G 133 | XP_016884744.1 | |
XM_017029256.1 | 566 | Missense Mutation | AGG,GGG | R,G 133 | XP_016884745.1 |