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ATGCTGGTTCTTACTGCTTTGTATT[G/T]TGTGTTCACTTCGCATGTATTAGGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609407 | ||||||||||||||||||||
Literature Links: |
HS3ST5 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 |
HS3ST5 - heparan sulfate-glucosamine 3-sulfotransferase 5 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_153612.3 | 2363 | Missense Mutation | AAA,CAA | K,Q 225 | NP_705840.2 | |
XM_006715379.2 | 2363 | Missense Mutation | AAA,CAA | K,Q 225 | XP_006715442.1 | |
XM_011535588.2 | 2363 | Missense Mutation | AAA,CAA | K,Q 225 | XP_011533890.1 | |
XM_017010470.1 | 2363 | Missense Mutation | AAA,CAA | K,Q 225 | XP_016865959.1 | |
XM_017010471.1 | 2363 | Missense Mutation | AAA,CAA | K,Q 225 | XP_016865960.1 | |
XM_017010472.1 | 2363 | Missense Mutation | AAA,CAA | K,Q 225 | XP_016865961.1 | |
XM_017010473.1 | 2363 | Missense Mutation | AAA,CAA | K,Q 225 | XP_016865962.1 | |
XM_017010474.1 | 2363 | Missense Mutation | AAA,CAA | K,Q 225 | XP_016865963.1 |
LOC101927768 - uncharacterized LOC101927768 | ||||||
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There are no transcripts associated with this gene. |