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CCAGTTATAAAGAGGTCACATAGTC[A/G]TGTGGGTCGAGGATTCTGTGCCTCC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 601530 | ||||||||||||||||||||
Literature Links: |
C5orf45 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 |
C5orf45 - chromosome 5 open reading frame 45 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001017987.2 | 861 | Missense Mutation | NP_001017987.1 | |||
NM_016175.3 | 861 | Missense Mutation | NP_057259.2 |
SQSTM1 - sequestosome 1 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001142298.1 | 861 | UTR 3 | NP_001135770.1 | |||
NM_001142299.1 | 861 | UTR 3 | NP_001135771.1 | |||
NM_003900.4 | 861 | UTR 3 | NP_003891.1 | |||
XM_011534683.2 | 861 | Intron | XP_011532985.1 | |||
XM_017010010.1 | 861 | Intron | XP_016865499.1 |