Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TCGATGTCCCCTCTTGGCTGGCCAG[C/G]GTTCCTGCTGGACTTCATTTCCTAC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605270 MIM: 610117 | ||||||||||||||||||||
Literature Links: |
SGSH 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 |
SGSH - N-sulfoglucosamine sulfohydrolase | ||||||
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There are no transcripts associated with this gene. |
SLC26A11 - solute carrier family 26 member 11 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001166347.1 | 809 | Missense Mutation | GCG,GGG | A,G 143 | NP_001159819.1 | |
NM_001166348.1 | 809 | Missense Mutation | GCG,GGG | A,G 143 | NP_001159820.1 | |
NM_001166349.1 | 809 | Missense Mutation | GCG,GGG | A,G 143 | NP_001159821.1 | |
NM_173626.3 | 809 | Missense Mutation | GCG,GGG | A,G 143 | NP_775897.3 | |
XM_006721833.1 | 809 | Missense Mutation | GCG,GGG | A,G 167 | XP_006721896.1 | |
XM_011524652.1 | 809 | Missense Mutation | CGT,GGT | R,G 50 | XP_011522954.1 | |
XM_011524653.1 | 809 | Missense Mutation | CGT,GGT | R,G 26 | XP_011522955.1 | |
XM_011524654.1 | 809 | Missense Mutation | CGT,GGT | R,G 26 | XP_011522956.1 | |
XM_017024505.1 | 809 | Missense Mutation | GCG,GGG | A,G 233 | XP_016879994.1 | |
XM_017024506.1 | 809 | Missense Mutation | GCG,GGG | A,G 233 | XP_016879995.1 | |
XM_017024507.1 | 809 | Missense Mutation | GCG,GGG | A,G 167 | XP_016879996.1 |