Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CGAGCTAGACAGCCACTTTCAGAAG[C/G]AAGTAACCAGCAGCCCCTCTCTGGT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616027 | ||||||||||||||||||||
Literature Links: |
ANLN 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 |
ANLN - anillin actin binding protein | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001284301.2 | 361 | Missense Mutation | GCA,GGA | A,G 47 | NP_001271230.1 | |
NM_001284302.2 | 361 | Missense Mutation | GCA,GGA | A,G 47 | NP_001271231.1 | |
NM_018685.4 | 361 | Missense Mutation | GCA,GGA | A,G 47 | NP_061155.2 | |
XM_006715746.1 | 361 | Missense Mutation | GCA,GGA | A,G 47 | XP_006715809.1 | |
XM_006715747.3 | 361 | Missense Mutation | GCA,GGA | A,G 47 | XP_006715810.1 | |
XM_017012354.1 | 361 | Missense Mutation | GCA,GGA | A,G 47 | XP_016867843.1 | |
XM_017012355.1 | 361 | Missense Mutation | GCA,GGA | A,G 47 | XP_016867844.1 | |
XM_017012356.1 | 361 | Missense Mutation | GCA,GGA | A,G 47 | XP_016867845.1 |
KIAA0895 - KIAA0895 | ||||||
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There are no transcripts associated with this gene. |