Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CGAGGTGCCCTTGCAGGTGACCGGG[C/T]GCCGCCTCTGGAAGAACGTGTACGA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611583 | ||||||||||||||||||||
Literature Links: |
ARID5A 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 |
ARID5A - AT-rich interaction domain 5A | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001319085.1 | 430 | Missense Mutation | CGC,TGC | R,C 162 | NP_001306014.1 | |
NM_001319087.1 | 430 | Missense Mutation | CGC,TGC | R,C 161 | NP_001306016.1 | |
NM_001319092.1 | 430 | Missense Mutation | CGC,TGC | R,C 40 | NP_001306021.1 | |
NM_001319093.1 | 430 | UTR 5 | NP_001306022.1 | |||
NM_001319094.1 | 430 | UTR 5 | NP_001306023.1 | |||
NM_001319096.1 | 430 | UTR 5 | NP_001306025.1 | |||
NM_212481.2 | 430 | Missense Mutation | CGC,TGC | R,C 108 | NP_997646.1 | |
XM_011510499.2 | 430 | Missense Mutation | CGC,TGC | R,C 118 | XP_011508801.1 | |
XM_017003183.1 | 430 | Missense Mutation | CGC,TGC | R,C 171 | XP_016858672.1 | |
XM_017003184.1 | 430 | Missense Mutation | CGC,TGC | R,C 56 | XP_016858673.1 | |
XM_017003185.1 | 430 | Missense Mutation | CGC,TGC | R,C 56 | XP_016858674.1 |