Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CCCCCTTTGTCAAGACGGCACGGGA[G/T]GGGGCGCAGACCAGCCTGCACTGCG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603930 MIM: 608830 MIM: 612012 | ||||||||||||||||||||
Literature Links: |
GPHN 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 |
RDH12 - retinol dehydrogenase 12 (all-trans/9-cis/11-cis) | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_152443.2 | 8082 | Missense Mutation | GAG,GAT | E,D 260 | NP_689656.2 |
ZFYVE26 - zinc finger FYVE-type containing 26 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_015346.3 | 8082 | Intron | NP_056161.2 | |||
XM_011536609.2 | 8082 | Intron | XP_011534911.1 | |||
XM_017021124.1 | 8082 | Intron | XP_016876613.1 | |||
XM_017021125.1 | 8082 | UTR 3 | XP_016876614.1 | |||
XM_017021126.1 | 8082 | Intron | XP_016876615.1 | |||
XM_017021127.1 | 8082 | Intron | XP_016876616.1 | |||
XM_017021128.1 | 8082 | Intron | XP_016876617.1 |