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CTGTGGATACATATTGCTGGCTTCA[C/T]AAAGGAGCTATTGCTTGTGCTGAAA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
6 submissions
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Phenotype: |
MIM: 606063 | ||||||||||||||||||||
Literature Links: |
EXO1 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 |
EXO1 - exonuclease 1 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001319224.1 | 422 | Silent Mutation | CAC,CAT | H,H 36 | NP_001306153.1 | |
NM_003686.4 | 422 | Silent Mutation | CAC,CAT | H,H 36 | NP_003677.4 | |
NM_006027.4 | 422 | Silent Mutation | CAC,CAT | H,H 36 | NP_006018.4 | |
NM_130398.3 | 422 | Silent Mutation | CAC,CAT | H,H 36 | NP_569082.2 | |
XM_006711840.2 | 422 | Silent Mutation | CAC,CAT | H,H 36 | XP_006711903.1 | |
XM_011544321.1 | 422 | Silent Mutation | CAC,CAT | H,H 36 | XP_011542623.1 | |
XM_011544322.1 | 422 | Silent Mutation | CAC,CAT | H,H 36 | XP_011542624.1 | |
XM_011544323.2 | 422 | Silent Mutation | CAC,CAT | H,H 36 | XP_011542625.1 | |
XM_011544324.2 | 422 | Silent Mutation | CAC,CAT | H,H 36 | XP_011542626.1 | |
XM_011544325.2 | 422 | Intron | XP_011542627.1 | |||
XM_017002793.1 | 422 | Silent Mutation | CAC,CAT | H,H 36 | XP_016858282.1 |