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ACAACGCTCTAAGAAGCAAGCACAC[C/T]GTCAGGCTGAGAAAACACTGGATAC
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 |
---|---|---|
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 |
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 | 1136 | Intron | NP_001032900.1 | |||
NM_004493.2 | 1136 | 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 | 1136 | Missense Mutation | CGT,TGT | R,C 300 | NP_001026915.1 | |
NM_001267053.3 | 1136 | Missense Mutation | CGT,TGT | R,C 185 | NP_001253982.1 | |
NM_144968.3 | 1136 | Intron | NP_659405.1 | |||
XM_005261988.3 | 1136 | Missense Mutation | CGT,TGT | R,C 300 | XP_005262045.1 | |
XM_005261990.3 | 1136 | Missense Mutation | CGT,TGT | R,C 185 | XP_005262047.1 |
SMC1A - structural maintenance of chromosomes 1A | ||||||
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There are no transcripts associated with this gene. |