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Search Thermo Fisher Scientific
CGTTCTCCGGCTGCCCTCCAGACTC[A/G]TGGAGGCGGTGTGCGAACTTGAGGA
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 |
---|---|---|
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 |
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 | 2184 | Missense Mutation | ACG,ATG | T,M 684 | NP_001244220.1 | |
NM_032591.2 | 2184 | Missense Mutation | ACG,ATG | T,M 683 | NP_115980.1 | |
XM_005272681.4 | 2184 | Missense Mutation | ACG,ATG | T,M 684 | XP_005272738.1 | |
XM_005272682.4 | 2184 | Missense Mutation | ACG,ATG | T,M 684 | XP_005272739.1 | |
XM_006724564.3 | 2184 | Missense Mutation | ACG,ATG | T,M 664 | XP_006724627.1 | |
XM_011543990.2 | 2184 | Missense Mutation | ACG,ATG | T,M 684 | XP_011542292.1 | |
XM_017029905.1 | 2184 | Missense Mutation | ACG,ATG | T,M 684 | XP_016885394.1 | |
XM_017029906.1 | 2184 | Missense Mutation | ACG,ATG | T,M 664 | XP_016885395.1 |