Variant #0000616153 (NC_000016.9:g.7759113del, NM_001142333.1:c.970del (RBFOX1))

Chromosome 16
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.7759113del
DNA change (hg38) g.7709111del
Published as -
ISCN -
DB-ID RBFOX1_000032
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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2022-05-09 15:24:52 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RBFOX1 NM_001142333.1 ?/. - c.970del r.(?) p.(Thr324ProfsTer7)
RBFOX1 NM_018723.3 ?/. - c.1051del r.(?) p.(Thr351ProfsTer7)


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