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TTGATGAGCTCAGAGCAGAATTTTA[C/T]TCAAAACATGCACACTTTCCCATGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606597 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
PAX3 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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PAX3 - paired box 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000438.5 | Intron | NP_000429.2 | ||||
NM_001127366.2 | Intron | NP_001120838.1 | ||||
NM_013942.4 | Intron | NP_039230.1 | ||||
NM_181457.3 | Intron | NP_852122.1 | ||||
NM_181458.3 | Intron | NP_852123.1 | ||||
NM_181459.3 | Intron | NP_852124.1 | ||||
NM_181460.3 | Intron | NP_852125.1 | ||||
NM_181461.3 | Intron | NP_852126.1 |