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CATTGACGGTTCAGCTAAAGTTAAC[A/G]TAACAGCAGCTGTTATGGAACTGGA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
2 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 |
---|---|---|
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 |
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 | 4031 | Missense Mutation | ACG,ATG | T,M 1291 | NP_001193723.1 | |
NM_016374.5 | 4031 | Missense Mutation | ACG,ATG | T,M 1291 | NP_057458.4 | |
NM_031371.3 | 4031 | Missense Mutation | ACG,ATG | T,M 1205 | NP_112739.2 | |
XM_006711781.2 | 4031 | Missense Mutation | ACG,ATG | T,M 1255 | XP_006711844.1 | |
XM_011544212.2 | 4031 | Missense Mutation | ACG,ATG | T,M 1291 | XP_011542514.1 | |
XM_017001468.1 | 4031 | Missense Mutation | ACG,ATG | T,M 1293 | XP_016856957.1 | |
XM_017001469.1 | 4031 | Missense Mutation | ACG,ATG | T,M 1257 | XP_016856958.1 | |
XM_017001470.1 | 4031 | Missense Mutation | ACG,ATG | T,M 1207 | XP_016856959.1 | |
XM_017001471.1 | 4031 | Intron | XP_016856960.1 | |||
XM_017001472.1 | 4031 | Missense Mutation | ACG,ATG | T,M 998 | XP_016856961.1 |
RBM34 - RNA binding motif protein 34 | ||||||
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There are no transcripts associated with this gene. |