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CAGTTTTGTTGAACTGTGAGAGCCT[C/T]CGTAGGAGCTTCTTCACGATTCCTG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610010 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ARSJ 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
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
|
ARSJ - arylsulfatase family member J | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_024590.3 | 3046 | Silent Mutation | CGA,CGG | R,R 521 | NP_078866.3 | |
XM_005263212.4 | 3046 | Silent Mutation | CGA,CGG | R,R 521 | XP_005263269.1 | |
XM_011532238.2 | 3046 | Silent Mutation | CGA,CGG | R,R 414 | XP_011530540.1 | |
XM_011532239.2 | 3046 | Silent Mutation | CGA,CGG | R,R 405 | XP_011530541.1 | |
XM_017008592.1 | 3046 | Silent Mutation | CGA,CGG | R,R 521 | XP_016864081.1 | |
XM_017008593.1 | 3046 | Silent Mutation | CGA,CGG | R,R 405 | XP_016864082.1 | |
XM_017008594.1 | 3046 | Silent Mutation | CGA,CGG | R,R 405 | XP_016864083.1 | |
XM_017008595.1 | 3046 | Silent Mutation | CGA,CGG | R,R 405 | XP_016864084.1 | |
XM_017008596.1 | 3046 | Silent Mutation | CGA,CGG | R,R 405 | XP_016864085.1 | |
XM_017008597.1 | 3046 | Silent Mutation | CGA,CGG | R,R 349 | XP_016864086.1 | |
XM_017008598.1 | 3046 | Silent Mutation | CGA,CGG | R,R 349 | XP_016864087.1 | |
XM_017008599.1 | 3046 | Silent Mutation | CGA,CGG | R,R 349 | XP_016864088.1 | |
XM_017008600.1 | 3046 | Silent Mutation | CGA,CGG | R,R 349 | XP_016864089.1 |