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Search Thermo Fisher Scientific
GTCATCACCCAGAAATTTATCATCC[A/G]TAAACTCAAACCCATGGATCCTAGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609835 | ||||||||||||||||||||
Literature Links: |
MYCBPAP 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 |
MYCBPAP - MYCBP associated protein | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_032133.4 | 403 | Missense Mutation | CAT,CGT | H,R 133 | NP_115509.4 | |
XM_005257725.3 | 403 | Missense Mutation | CAT,CGT | H,R 133 | XP_005257782.1 | |
XM_005257726.2 | 403 | Missense Mutation | CAT,CGT | H,R 133 | XP_005257783.1 | |
XM_011525342.1 | 403 | Missense Mutation | CAT,CGT | H,R 133 | XP_011523644.1 | |
XM_011525343.1 | 403 | Missense Mutation | CAT,CGT | H,R 133 | XP_011523645.1 | |
XM_017025205.1 | 403 | Missense Mutation | CAT,CGT | H,R 133 | XP_016880694.1 |