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GCACTTCCTCCGAGCTGCTCTTCGT[C/T]CTCCGGCTGCCCTCCAGACTCGTGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 300375 MIM: 300368 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CHST7 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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CHST7 - carbohydrate sulfotransferase 7 | ||||||
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There are no transcripts associated with this gene. |
SLC9A7 - solute carrier family 9 member A7 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001257291.1 | 2206 | Silent Mutation | AGA,AGG | R,R 691 | NP_001244220.1 | |
NM_032591.2 | 2206 | Silent Mutation | AGA,AGG | R,R 690 | NP_115980.1 | |
XM_005272681.4 | 2206 | Silent Mutation | AGA,AGG | R,R 691 | XP_005272738.1 | |
XM_005272682.4 | 2206 | Silent Mutation | AGA,AGG | R,R 691 | XP_005272739.1 | |
XM_006724564.3 | 2206 | Silent Mutation | AGA,AGG | R,R 671 | XP_006724627.1 | |
XM_011543990.2 | 2206 | Silent Mutation | AGA,AGG | R,R 691 | XP_011542292.1 | |
XM_017029905.1 | 2206 | Silent Mutation | AGA,AGG | R,R 691 | XP_016885394.1 | |
XM_017029906.1 | 2206 | Silent Mutation | AGA,AGG | R,R 671 | XP_016885395.1 |