Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 114025 MIM: 610867 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
CTNNA2 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)
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EAS
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African American - Not Available | YRI (Yoruba)
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SAS
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Chinese - Not Available | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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CTNNA2 - catenin alpha 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001164883.1 | 1259 | Intron | NP_001158355.1 | |||
NM_001282597.2 | 1259 | Intron | NP_001269526.1 | |||
NM_001282598.1 | 1259 | Intron | NP_001269527.1 | |||
NM_001282599.1 | 1259 | Intron | NP_001269528.1 | |||
NM_001282600.1 | 1259 | Intron | NP_001269529.1 | |||
NM_001320810.1 | 1259 | Intron | NP_001307739.1 | |||
NM_004389.3 | 1259 | Intron | NP_004380.2 | |||
XM_011532555.2 | 1259 | Intron | XP_011530857.1 | |||
XM_011532556.2 | 1259 | Intron | XP_011530858.1 | |||
XM_011532557.2 | 1259 | Intron | XP_011530859.1 | |||
XM_017003403.1 | 1259 | Intron | XP_016858892.1 | |||
XM_017003404.1 | 1259 | Intron | XP_016858893.1 | |||
XM_017003405.1 | 1259 | Intron | XP_016858894.1 | |||
XM_017003406.1 | 1259 | Intron | XP_016858895.1 |
LRRTM1 - leucine rich repeat transmembrane neuronal 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_178839.4 | 1259 | Missense Mutation | AAC,AGC | N,S 330 | NP_849161.2 | |
XM_017003986.1 | 1259 | Missense Mutation | AAC,AGC | N,S 330 | XP_016859475.1 | |
XM_017003987.1 | 1259 | Missense Mutation | AAC,AGC | N,S 330 | XP_016859476.1 |
Set Membership: |
HapMap |