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InDels (insertion-deletion)

Please enter a gene symbol or a chrom location to obtain InDels information and InDels Frequency distribution of sheep breeds or core group worldwide.

Basic Search

dbSNP rsid:   (e.g.rs430448688)

Or   Gene symbol:   (e.g. NR6A1, LCORLi, DGAT1)

Or Chrom location:   (e.g. 3:11130000-11160000 or 9:13560000)

Advanced Search

Minor Allele Frequency    (range: 0-1)

Consequence Type:

Gene Variant
  • Coding Variant
    • frameshift_variant
    • exon_loss_variant
    • gene_fusion
    • bidirectional_gene_fusion
    • start_lost
    • stop_gained
    • stop_lost
    • conservative_inframe_deletion
    • conservative_inframe_insertion
    • disruptive_inframe_deletion
    • disruptive_inframe_insertion
  • Non-coding Variant
    • 5_prime_UTR_variant
    • 3_prime_UTR_variant
    • intron_variant
    • intron_splicing_variant
    • non_coding_transcript_exon_variant
  • Splice Variant
    • splice_acceptor_variant
    • splice_donor_variant
    • splice_region_variant
Intergenic Variant
  • upstream_gene_variant
  • downstream_gene_variant
  • intergenic_variant
Intragenic Variant
  • intragenic_variant