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CGGAAGGGGTTCATGTCATTGAAGG[C/T]GATGTTCATCAGCTTCCTGGGAGGA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602159 MIM: 609871 | ||||||||||||||||||||
Literature Links: |
CORO2A 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 |
CORO2A - coronin 2A | ||||||
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There are no transcripts associated with this gene. |
TBC1D2 - TBC1 domain family member 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001267571.1 | 2776 | Missense Mutation | ACC,GCC | T,A 866 | NP_001254500.1 | |
NM_001267572.1 | 2776 | Missense Mutation | ACC,GCC | T,A 406 | NP_001254501.1 | |
NM_018421.3 | 2776 | Missense Mutation | ACC,GCC | T,A 855 | NP_060891.3 | |
XM_011518843.1 | 2776 | Missense Mutation | ACC,GCC | T,A 406 | XP_011517145.1 | |
XM_011518844.2 | 2776 | Intron | XP_011517146.1 | |||
XM_017014899.1 | 2776 | Missense Mutation | ACC,GCC | T,A 421 | XP_016870388.1 |