Phenotype–resequencing pairing is incomplete: a verified crosswalk between paper Rxx IDs and public F1-xx / 164L / X5H IDs is missing. Number or row order is not used to guess identities. Variant and source phenotype records remain separate; matched-sample joint analysis is unavailable. Integration status
CRA009020 · PASS SNP / INDEL
Gene-level variant query
Enter a gene ID to view candidate SNPs/INDELs in the OH1004 and TK1151 reference coordinates and carriers among 129 CRA009020 resequenced samples: 127 F1 offspring plus parents 164L and X5H. These are not 129 independent varieties.
Task is running normally, please waitElapsed 00:00
Enter a gene ID or genomic interval to begin.