Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CCACAGGGAAAGGGCTTGGTGCAGC[C/T]TCCCTCACAACACACACGTCATTCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
3 submissions
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Phenotype: |
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Literature Links: |
SUCO 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 |
SUCO - SUN domain containing ossification factor | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001282750.1 | 219 | Intron | NP_001269679.1 | |||
NM_001282751.1 | 219 | Intron | NP_001269680.1 | |||
NM_014283.4 | 219 | Intron | NP_055098.1 | |||
NM_016227.3 | 219 | Missense Mutation | CCT,CTT | P,L 32 | NP_057311.3 | |
XM_006711374.2 | 219 | Intron | XP_006711437.1 | |||
XM_006711375.2 | 219 | Intron | XP_006711438.1 | |||
XM_006711376.1 | 219 | Intron | XP_006711439.1 |