Variant #0000473816 (NC_000017.10:g.76989790del, NM_001159772.1:c.1048del (CANT1))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method ACMG
Clinical classification pathogenic (recessive)
DNA change (genomic) (Relative to hg19 / GRCh37) g.76989790del
DNA change (hg38) g.78993708del
Published as -
ISCN -
DB-ID CANT1_000014
Variant remarks Desbuquois Dysplasia
Reference -
ClinVar ID -
dbSNP ID rs1294064847
Origin Unknown
Segregation yes
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 View details
Owner Cynthia Silveira
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Cynthia Silveira
Date created 2019-04-18 16:24:03 +02:00 (CEST)
Date last edited 2021-09-09 14:41:03 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CANT1 NM_001159772.1 +?/. 3 c.1048del r.(?) p.(Ile350Serfs*44)


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