Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CTGGACGCCATCACCGATAAGGACC[C/T]CCTGGTGCAGGAGCAGGTCTGCAGT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
MROH1 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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MROH1 - maestro heat like repeat family member 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001099280.2 | 302 | Missense Mutation | CCC,CTC | P,L 22 | NP_001092750.1 | |
NM_001099281.2 | 302 | Missense Mutation | CCC,CTC | P,L 22 | NP_001092751.1 | |
NM_001288814.1 | 302 | Missense Mutation | CCC,CTC | P,L 22 | NP_001275743.1 | |
NM_032450.2 | 302 | Missense Mutation | CCC,CTC | P,L 22 | NP_115826.2 | |
XM_011517270.2 | 302 | Missense Mutation | CCC,CTC | P,L 115 | XP_011515572.1 | |
XM_011517271.2 | 302 | Missense Mutation | CCC,CTC | P,L 115 | XP_011515573.1 | |
XM_011517272.2 | 302 | Missense Mutation | CCC,CTC | P,L 115 | XP_011515574.1 | |
XM_011517273.2 | 302 | Missense Mutation | CCC,CTC | P,L 115 | XP_011515575.1 | |
XM_011517274.2 | 302 | Missense Mutation | CCC,CTC | P,L 115 | XP_011515576.1 | |
XM_011517275.2 | 302 | Missense Mutation | CCC,CTC | P,L 115 | XP_011515577.1 | |
XM_011517276.2 | 302 | Missense Mutation | CCC,CTC | P,L 22 | XP_011515578.1 | |
XM_011517277.1 | 302 | Missense Mutation | CCC,CTC | P,L 22 | XP_011515579.1 | |
XM_011517278.1 | 302 | Missense Mutation | CCC,CTC | P,L 22 | XP_011515580.1 | |
XM_011517279.2 | 302 | Missense Mutation | CCC,CTC | P,L 22 | XP_011515581.1 | |
XM_011517281.1 | 302 | Intron | XP_011515583.1 | |||
XM_011517282.1 | 302 | Intron | XP_011515584.1 | |||
XM_011517283.2 | 302 | Missense Mutation | CCC,CTC | P,L 22 | XP_011515585.1 | |
XM_011517285.1 | 302 | Missense Mutation | CCC,CTC | P,L 22 | XP_011515587.1 | |
XM_011517286.2 | 302 | Missense Mutation | CCC,CTC | P,L 115 | XP_011515588.1 | |
XM_017013802.1 | 302 | Missense Mutation | CCC,CTC | P,L 115 | XP_016869291.1 | |
XM_017013803.1 | 302 | Missense Mutation | CCC,CTC | P,L 115 | XP_016869292.1 | |
XM_017013804.1 | 302 | Missense Mutation | CCC,CTC | P,L 22 | XP_016869293.1 | |
XM_017013805.1 | 302 | Missense Mutation | CCC,CTC | P,L 22 | XP_016869294.1 | |
XM_017013806.1 | 302 | Intron | XP_016869295.1 | |||
XM_017013807.1 | 302 | Missense Mutation | CCC,CTC | P,L 115 | XP_016869296.1 |