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GAATAATAATCAAAATGATTATTCC[A/G]GTCTCAGTGATTCCCAGTTCCTCTT
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
CCDC36 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 - 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 |
CCDC36 - coiled-coil domain containing 36 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001135197.1 | 201 | Missense Mutation | AGT,GGT | S,G 35 | NP_001128669.1 | |
NM_178173.3 | 201 | Missense Mutation | AGT,GGT | S,G 35 | NP_835467.2 | |
XM_006713124.3 | 201 | Missense Mutation | AGT,GGT | S,G 35 | XP_006713187.1 | |
XM_011533670.2 | 201 | Missense Mutation | AGT,GGT | S,G 42 | XP_011531972.1 | |
XM_011533671.2 | 201 | Missense Mutation | AGT,GGT | S,G 42 | XP_011531973.1 | |
XM_011533672.2 | 201 | Missense Mutation | AGT,GGT | S,G 35 | XP_011531974.1 | |
XM_011533673.2 | 201 | Missense Mutation | AGT,GGT | S,G 35 | XP_011531975.1 |