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CATGACTCCAGAGCAGCAAGCTGCC[A/T]TCAGGAAAGAGCAGGAAGTACAACG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 300256 MIM: 300040 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
HSD17B10 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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HSD17B10 - hydroxysteroid 17-beta dehydrogenase 10 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001037811.2 | 1091 | Intron | NP_001032900.1 | |||
NM_004493.2 | 1091 | Intron | NP_004484.1 |
RIBC1 - RIB43A domain with coiled-coils 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001031745.4 | 1091 | Missense Mutation | ATC,TTC | I,F 285 | NP_001026915.1 | |
NM_001267053.3 | 1091 | Missense Mutation | ATC,TTC | I,F 170 | NP_001253982.1 | |
NM_144968.3 | 1091 | Intron | NP_659405.1 | |||
XM_005261988.3 | 1091 | Missense Mutation | ATC,TTC | I,F 285 | XP_005262045.1 | |
XM_005261990.3 | 1091 | Missense Mutation | ATC,TTC | I,F 170 | XP_005262047.1 |
SMC1A - structural maintenance of chromosomes 1A | ||||||
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There are no transcripts associated with this gene. |