Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GCCAGCTGATGTGTCCCGACACTGC[C/T]CGGTGAAGGTTGGACCCGGGAGGGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616157 | ||||||||||||||||||||
Literature Links: |
DHRS13 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 |
DHRS13 - dehydrogenase/reductase 13 | ||||||
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There are no transcripts associated with this gene. |
PHF12 - PHD finger protein 12 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001033561.1 | 2150 | Missense Mutation | AGC,GGC | S,G 771 | NP_001028733.1 | |
NM_001290131.1 | 2150 | Missense Mutation | AGC,GGC | S,G 771 | NP_001277060.1 | |
NM_020889.2 | 2150 | Intron | NP_065940.1 | |||
XM_005258015.3 | 2150 | Missense Mutation | AGC,GGC | S,G 681 | XP_005258072.1 | |
XM_005258016.3 | 2150 | Missense Mutation | AGC,GGC | S,G 554 | XP_005258073.1 | |
XM_011525078.2 | 2150 | Missense Mutation | AGC,GGC | S,G 749 | XP_011523380.1 | |
XM_011525079.2 | 2150 | Missense Mutation | AGC,GGC | S,G 771 | XP_011523381.1 | |
XM_011525082.2 | 2150 | Intron | XP_011523384.1 | |||
XM_011525083.2 | 2150 | Intron | XP_011523385.1 | |||
XM_017024903.1 | 2150 | Missense Mutation | AGC,GGC | S,G 789 | XP_016880392.1 | |
XM_017024904.1 | 2150 | Missense Mutation | AGC,GGC | S,G 740 | XP_016880393.1 |