Search Thermo Fisher Scientific
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TCCATTTCCAAGTTCTGATTCATAA[A/G]AGCTTCCAAAGTAGAGCCGGTACAT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 614518 MIM: 602136 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
GATAD1 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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GATAD1 - GATA zinc finger domain containing 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_021167.4 | 3529 | Intron | NP_066990.3 |
PEX1 - peroxisomal biogenesis factor 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000466.2 | 3529 | Missense Mutation | TCT,TTT | S,F 1133 | NP_000457.1 | |
NM_001282677.1 | 3529 | Missense Mutation | TCT,TTT | S,F 1076 | NP_001269606.1 | |
NM_001282678.1 | 3529 | Missense Mutation | TCT,TTT | S,F 925 | NP_001269607.1 | |
XM_017012319.1 | 3529 | Missense Mutation | TCT,TTT | S,F 550 | XP_016867808.1 |