Variant #0000276155 (NC_000017.10:g.77082105C>A, NM_001082575.1:c.*4860G>T (RBFOX3))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.77082105C>A
DNA change (hg38) g.79086023C>A
Published as ENGASE(NM_001042573.2):c.1906C>A (p.R636=)
ISCN -
DB-ID ENGASE_000002
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ENGASE NM_001042573.2 -?/. - c.1906C>A r.(?) p.(Arg636=)
RBFOX3 NM_001082575.1 -?/. - c.*4860G>T r.(=) p.(=)


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