Variant #0000546015 (NC_000011.9:g.86666089_86666098del, NM_012193.3:c.40_49del (FZD4))

Chromosome 11
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.86666089_86666098del
DNA change (hg38) g.86955047_86955056del
Published as -
ISCN -
DB-ID FZD4_000050 See all 6 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-01 11:04:12 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PRSS23 NM_007173.4 +/. - c.*146252_*146261del r.(=) p.(=)
FZD4 NM_012193.3 +/. - c.40_49del r.(?) p.(Pro14SerfsTer44)


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