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AAGCCTGAGTAGGGCACCGCATTGG[C/T]GCTTGGGGAACCTTGAGTAGGAAAT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 180903 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
LOC101928134 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)
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EAS
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African American - Not Available | YRI (Yoruba)
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SAS
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Chinese - Not Available | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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LOC101928134 - uncharacterized LOC101928134 | ||||||
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There are no transcripts associated with this gene. |
RYR3 - ryanodine receptor 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001036.4 | Intron | NP_001027.3 | ||||
NM_001243996.2 | Intron | NP_001230925.1 | ||||
XM_011521880.2 | Intron | XP_011520182.1 | ||||
XM_017022468.1 | Intron | XP_016877957.1 | ||||
XM_017022469.1 | Intron | XP_016877958.1 | ||||
XM_017022470.1 | Intron | XP_016877959.1 | ||||
XM_017022471.1 | Intron | XP_016877960.1 | ||||
XM_017022472.1 | Intron | XP_016877961.1 | ||||
XM_017022473.1 | Intron | XP_016877962.1 | ||||
XM_017022474.1 | Intron | XP_016877963.1 | ||||
XM_017022475.1 | Intron | XP_016877964.1 | ||||
XM_017022476.1 | Intron | XP_016877965.1 | ||||
XM_017022477.1 | Intron | XP_016877966.1 |
Set Membership: |
HapMap |