Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GATGGGCATCTCTGCTGAAAAGGTA[C/G]CTGCCATATTATCACCAGAGTACGA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
INO80D 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 |
INO80D - INO80 complex subunit D | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_017759.4 | 2810 | Missense Mutation | GCT,GGT | A,G 858 | NP_060229.3 | |
XM_011511369.2 | 2810 | Missense Mutation | GCT,GGT | A,G 887 | XP_011509671.1 | |
XM_011511370.2 | 2810 | Missense Mutation | GCT,GGT | A,G 858 | XP_011509672.1 | |
XM_011511371.2 | 2810 | Missense Mutation | GCT,GGT | A,G 858 | XP_011509673.1 | |
XM_011511373.2 | 2810 | Missense Mutation | GCT,GGT | A,G 858 | XP_011509675.1 | |
XM_011511375.2 | 2810 | Missense Mutation | GCT,GGT | A,G 753 | XP_011509677.1 | |
XM_011511376.2 | 2810 | Missense Mutation | GCT,GGT | A,G 753 | XP_011509678.1 |