Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
ATGGTGGCAGCAGTGGCAGTGATGG[C/T]GGCAGCAGTGGCGGCAGCAGCAACT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 300410 | ||||||||||||||||||||
Literature Links: |
AMOT 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 |
AMOT - angiomotin | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001113490.1 | 2456 | Missense Mutation | ACC,GCC | T,A 895 | NP_001106962.1 | |
NM_133265.2 | 2456 | Missense Mutation | ACC,GCC | T,A 486 | NP_573572.1 | |
XM_005262087.1 | 2456 | Missense Mutation | ACC,GCC | T,A 895 | XP_005262144.1 | |
XM_005262090.1 | 2456 | Missense Mutation | ACC,GCC | T,A 486 | XP_005262147.1 | |
XM_011530875.2 | 2456 | Missense Mutation | ACC,GCC | T,A 895 | XP_011529177.1 | |
XM_017029289.1 | 2456 | Missense Mutation | ACC,GCC | T,A 486 | XP_016884778.1 |
MIR4329 - microRNA 4329 | ||||||
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There are no transcripts associated with this gene. |