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TCTTCACCCACAGGTTTAGGTTTTA[A/G]CTGGCTGCTCAGTGTTAAAAAGGAA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605573 MIM: 609182 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
HSD17B3 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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HSD17B3 - hydroxysteroid 17-beta dehydrogenase 3 | ||||||
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There are no transcripts associated with this gene. |
SLC35D2 - solute carrier family 35 member D2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001286990.1 | 1037 | Silent Mutation | CTA,TTA | L,L 233 | NP_001273919.1 | |
NM_007001.2 | 1037 | Silent Mutation | CTA,TTA | L,L 321 | NP_008932.2 | |
XM_005251673.1 | 1037 | Missense Mutation | GCT,GTT | A,V 298 | XP_005251730.1 | |
XM_005251674.1 | 1037 | Missense Mutation | GCT,GTT | A,V 293 | XP_005251731.1 | |
XM_005251675.2 | 1037 | Silent Mutation | CTA,TTA | L,L 274 | XP_005251732.1 | |
XM_005251676.1 | 1037 | UTR 3 | XP_005251733.1 | |||
XM_005251678.4 | 1037 | Silent Mutation | CTA,TTA | L,L 203 | XP_005251735.1 | |
XM_006716939.2 | 1037 | Silent Mutation | CTA,TTA | L,L 186 | XP_006717002.1 | |
XM_011518164.1 | 1037 | Silent Mutation | CTA,TTA | L,L 264 | XP_011516466.1 |