Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GGGGCGCAGACCAGCCTGCACTGCG[C/G]CCTGGCTGAGGGCCTGGAGCCCCTG
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 | |||
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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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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 | 8056 | Missense Mutation | GCC,GGC | A,G 269 | 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 | 8056 | Intron | NP_056161.2 | |||
XM_011536609.2 | 8056 | Intron | XP_011534911.1 | |||
XM_017021124.1 | 8056 | Intron | XP_016876613.1 | |||
XM_017021125.1 | 8056 | UTR 3 | XP_016876614.1 | |||
XM_017021126.1 | 8056 | Intron | XP_016876615.1 | |||
XM_017021127.1 | 8056 | Intron | XP_016876616.1 | |||
XM_017021128.1 | 8056 | Intron | XP_016876617.1 |