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TGTAGCACTGGTTATAGCCCCCACT[C/G]TCTTACTGACAATGCTTTCTTCTGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607667 MIM: 610869 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CTNNA3 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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CTNNA3 - catenin alpha 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001127384.2 | 614 | Intron | NP_001120856.1 | |||
NM_001291133.1 | 614 | Intron | NP_001278062.1 | |||
NM_013266.3 | 614 | Intron | NP_037398.2 | |||
XM_017016151.1 | 614 | Intron | XP_016871640.1 | |||
XM_017016152.1 | 614 | Intron | XP_016871641.1 | |||
XM_017016153.1 | 614 | Intron | XP_016871642.1 | |||
XM_017016154.1 | 614 | Intron | XP_016871643.1 | |||
XM_017016155.1 | 614 | Intron | XP_016871644.1 | |||
XM_017016156.1 | 614 | Intron | XP_016871645.1 | |||
XM_017016157.1 | 614 | Intron | XP_016871646.1 | |||
XM_017016158.1 | 614 | Intron | XP_016871647.1 |
LOC101928961 - uncharacterized LOC101928961 | ||||||
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There are no transcripts associated with this gene. |
LRRTM3 - leucine rich repeat transmembrane neuronal 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_178011.4 | 614 | Missense Mutation | CTC,GTC | L,V 22 | NP_821079.3 |