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GACACCATCAGCGATTCCAGGTTTC[C/T]AGCCCCTGGGCCCCAAGGAACCTTT
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 | |||
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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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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 | Intron | NP_001159819.1 | ||||
NM_001166348.1 | Intron | NP_001159820.1 | ||||
NM_001166349.1 | Intron | NP_001159821.1 | ||||
NM_173626.3 | Intron | NP_775897.3 | ||||
XM_006721833.1 | Intron | XP_006721896.1 | ||||
XM_011524652.1 | Intron | XP_011522954.1 | ||||
XM_011524653.1 | Intron | XP_011522955.1 | ||||
XM_011524654.1 | Intron | XP_011522956.1 | ||||
XM_017024505.1 | Intron | XP_016879994.1 | ||||
XM_017024506.1 | Intron | XP_016879995.1 | ||||
XM_017024507.1 | Intron | XP_016879996.1 |