Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TTTTCCAAACAATTTGAATGTTGCT[A/G]TTGGAAGTTCTAGGTTACCTCCTTC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
CCDC15 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 |
CCDC15 - coiled-coil domain containing 15 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_025004.2 | 1821 | Missense Mutation | ATT,GTT | I,V 141 | NP_079280.2 | |
XM_017018346.1 | 1821 | Missense Mutation | ATT,GTT | I,V 141 | XP_016873835.1 | |
XM_017018347.1 | 1821 | Missense Mutation | ATT,GTT | I,V 141 | XP_016873836.1 | |
XM_017018348.1 | 1821 | Missense Mutation | ATT,GTT | I,V 141 | XP_016873837.1 | |
XM_017018349.1 | 1821 | Missense Mutation | ATT,GTT | I,V 92 | XP_016873838.1 | |
XM_017018350.1 | 1821 | Missense Mutation | ATT,GTT | I,V 141 | XP_016873839.1 | |
XM_017018351.1 | 1821 | Missense Mutation | ATT,GTT | I,V 141 | XP_016873840.1 | |
XM_017018352.1 | 1821 | Missense Mutation | ATT,GTT | I,V 24 | XP_016873841.1 | |
XM_017018353.1 | 1821 | Missense Mutation | ATT,GTT | I,V 141 | XP_016873842.1 |