Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
ATGGAAACTACAGTGTCCAGACCGG[C/T]CCTTTCTCCAACCCACATCAACGCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
CCDC150 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 |
CCDC150 - coiled-coil domain containing 150 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001080539.1 | 179 | Missense Mutation | GCC,GTC | A,V 15 | NP_001074008.1 | |
XM_006712438.3 | 179 | Missense Mutation | GCC,GTC | A,V 15 | XP_006712501.1 | |
XM_006712439.3 | 179 | Intron | XP_006712502.1 | |||
XM_011510985.2 | 179 | Intron | XP_011509287.1 | |||
XM_011510987.2 | 179 | Intron | XP_011509289.1 | |||
XM_011510988.2 | 179 | Intron | XP_011509290.1 | |||
XM_017003861.1 | 179 | Missense Mutation | GCC,GTC | A,V 15 | XP_016859350.1 | |
XM_017003862.1 | 179 | Missense Mutation | GCC,GTC | A,V 15 | XP_016859351.1 | |
XM_017003863.1 | 179 | Missense Mutation | GCC,GTC | A,V 15 | XP_016859352.1 | |
XM_017003864.1 | 179 | Missense Mutation | GCC,GTC | A,V 15 | XP_016859353.1 | |
XM_017003865.1 | 179 | Intron | XP_016859354.1 | |||
XM_017003866.1 | 179 | Intron | XP_016859355.1 |