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CCTTCCTGGGAACAGTCATAATAAT[A/G]GGTTCACACTTTCTCTCATGAAGTT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605269 | ||||||||||||||||||||
Literature Links: |
CORO1C 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 |
CORO1C - coronin 1C | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001105237.2 | 1243 | Silent Mutation | CCC,CCT | P,P 398 | NP_001098707.1 | |
NM_001276471.1 | 1243 | Silent Mutation | CCC,CCT | P,P 345 | NP_001263400.1 | |
NM_014325.3 | 1243 | Silent Mutation | CCC,CCT | P,P 345 | NP_055140.1 | |
XM_011538125.1 | 1243 | Silent Mutation | CCC,CCT | P,P 157 | XP_011536427.1 | |
XM_017019121.1 | 1243 | Silent Mutation | CCC,CCT | P,P 398 | XP_016874610.1 | |
XM_017019122.1 | 1243 | Silent Mutation | CCC,CCT | P,P 345 | XP_016874611.1 | |
XM_017019123.1 | 1243 | Silent Mutation | CCC,CCT | P,P 345 | XP_016874612.1 |