Allele/Variant

a356

Species
Danio rerio
Symbol
a356
Category
allele
Allele of gene
cnksr2b
Transgenic Constructs
None
Synonyms
None
Description
Not Available
Additional Information
Literature

Transgenic Constructs

No data available

Genomic Variant Information

NC_007132.7:g.25484327_25484452delinsT

Symbol
NC_007132.7:g.25484327_25484452delinsT
Category
Variant
Variant type
delins
Overlaps
cnksr2b
Location
21:25484327-25484452
Nucleotide Change
CTTGGCGGCAGCGATGAGGTCCACGACAGAAGTCAGGAAGTCATTAGGAAGTTTTCGGGTGGCTCTGCCATCATAGTGTCCACCCCTCCGCCGGCCTGTTATGAAGTTCTGTAGGTTCTTGGCTGA>T
Most Severe Consequence
  • frameshift variant
See all consequences
HGVS.g name
  • 21:g.25484327_25484452delinsT
  • NC_007132.7:g.25484327_25484452delinsT
HGVS.c name
  • ENSEMBL:ENSDART00000110923.1:c.283_408delinsA
  • ENSEMBL:ENSDART00000162711.1:c.283_408delinsA
HGVS.p name
  • :p.Ser95LysfsTer8
Synonyms
Not Available
Notes
Not Available
Cross references
Not Available
References
All alleles with this variant

Genome location
Assembly version
GRCz11
Viewer Help
25.43M25.44M25.45M25.46M25.47M25.48M25.49M25.50M25.51M25.52M
Variant Types and ConsequencesOnly variants associated to alleles are shown in the graphics above. See all variants in JBrowse.

Variant Molecular Consequences

Predicted effect of NC_007132.7:g.25484327_25484452delinsT

Variant
NC_007132.7:g.25484327_25484452delinsT
Variant type:
delins
Sequence feature
Sequence feature type
Associated gene
Location
Molecular consequence
Codon and amino acid change
No records match query. Try removing filters.
Showing 0 - 0 of 0 rows
per page

    Phenotypes

    No data available

    Disease Associations

    No data available