Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AGCCGCCTTGCTATAGTCTCATTAC[A/G]AGCTTGGGCAGAGACCCATGCCACA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603930 MIM: 607849 MIM: 603207 | ||||||||||||||||||||
Literature Links: |
GPHN PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
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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 |
RDH11 - retinol dehydrogenase 11 (all-trans/9-cis/11-cis) | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001252650.1 | 979 | Missense Mutation | CGT,TGT | R,C 227 | NP_001239579.1 | |
NM_016026.3 | 979 | Missense Mutation | CGT,TGT | R,C 297 | NP_057110.3 |
VTI1B - vesicle transport through interaction with t-SNAREs 1B | ||||||
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There are no transcripts associated with this gene. |