Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TCCAGAAAATTCAGTCCCTCAATAC[A/G]CTTTTGAATTTCCTCATTGATCTCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 300545 | ||||||||||||||||||||
Literature Links: |
HS6ST2 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 |
HS6ST2 - heparan sulfate 6-O-sulfotransferase 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001077188.1 | 1962 | Missense Mutation | CGT,TGT | R,C 516 | NP_001070656.1 | |
NM_147175.3 | 1962 | Missense Mutation | CGT,TGT | R,C 476 | NP_671704.3 | |
XM_005262490.3 | 1962 | Missense Mutation | CGT,TGT | R,C 516 | XP_005262547.1 | |
XM_005262491.2 | 1962 | Missense Mutation | CGT,TGT | R,C 487 | XP_005262548.1 | |
XM_011531406.1 | 1962 | Missense Mutation | CGT,TGT | R,C 370 | XP_011529708.1 | |
XM_011531407.2 | 1962 | Intron | XP_011529709.1 | |||
XM_011531408.2 | 1962 | Intron | XP_011529710.1 | |||
XM_017029944.1 | 1962 | Missense Mutation | CGT,TGT | R,C 476 | XP_016885433.1 | |
XM_017029945.1 | 1962 | Missense Mutation | CGT,TGT | R,C 370 | XP_016885434.1 | |
XM_017029946.1 | 1962 | Missense Mutation | CGT,TGT | R,C 341 | XP_016885435.1 |