Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CTCCCTCACCGGCCCTTGGACTCCC[C/T]GTACGTGTTTCGGGCCATTGACACC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 612856 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ASTN2 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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ASTN2 - astrotactin 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001184734.1 | 1392 | Intron | NP_001171663.1 | |||
NM_001184735.1 | 1392 | Intron | NP_001171664.1 | |||
NM_014010.4 | 1392 | Missense Mutation | AGG,GGG | R,G 1283 | NP_054729.3 | |
NM_198186.3 | 1392 | Missense Mutation | AGG,GGG | R,G 435 | NP_937829.3 | |
NM_198187.3 | 1392 | Missense Mutation | AGG,GGG | R,G 386 | NP_937830.3 | |
NM_198188.2 | 1392 | Intron | NP_937831.1 |