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GGCACTTGTCATATTTTCCAGGTCC[A/G]CTATAAATTTAAAGCTTTCATTAAC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
4 submissions
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Phenotype: |
MIM: 609696 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ARID4B 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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ARID4B - AT-rich interaction domain 4B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001206794.1 | 3824 | Missense Mutation | TCG,TTG | S,L 1222 | NP_001193723.1 | |
NM_016374.5 | 3824 | Missense Mutation | TCG,TTG | S,L 1222 | NP_057458.4 | |
NM_031371.3 | 3824 | Missense Mutation | TCG,TTG | S,L 1136 | NP_112739.2 | |
XM_006711781.2 | 3824 | Missense Mutation | TCG,TTG | S,L 1186 | XP_006711844.1 | |
XM_011544212.2 | 3824 | Missense Mutation | TCG,TTG | S,L 1222 | XP_011542514.1 | |
XM_017001468.1 | 3824 | Missense Mutation | TCG,TTG | S,L 1224 | XP_016856957.1 | |
XM_017001469.1 | 3824 | Missense Mutation | TCG,TTG | S,L 1188 | XP_016856958.1 | |
XM_017001470.1 | 3824 | Missense Mutation | TCG,TTG | S,L 1138 | XP_016856959.1 | |
XM_017001471.1 | 3824 | Intron | XP_016856960.1 | |||
XM_017001472.1 | 3824 | Missense Mutation | TCG,TTG | S,L 929 | XP_016856961.1 |