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Date: Fri Dec 13 2024
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a356
ZFIN:ZDB-ALT-200205-13
Allele of
cnksr2b
Danio rerio
Summary
Transgenic Constructs
Genomic Variant Information
Variant Molecular Consequences
Phenotypes
Disease Associations
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
Show All 3
HGVS.c name
ENSEMBL:ENSDART00000110923.1:c.283_408delinsA
ENSEMBL:ENSDART00000162711.1:c.283_408delinsA
Show All 3
HGVS.p name
:p.Ser95LysfsTer8
Synonyms
Not Available
Notes
Not Available
Cross references
Not Available
References
PMID:30929901
All alleles with this variant
Download Variants Data
Genome location
Chr21:25425964...25522906
(96.94 kb)
Assembly version
GRCz11
Viewer Help
25.43M
25.44M
25.45M
25.46M
25.47M
25.48M
25.49M
25.50M
25.51M
25.52M
Variant Types and Consequences
Only 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
Show all details
Sequence feature
Sequence feature type
Associated gene
Location
Molecular consequence
Codon and amino acid change
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Phenotypes
No data available
Disease Associations
No data available
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