Variant #0001002594 (NC_000016.9:g.7759113A>C, NM_001142333.1:c.970A>C (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.7759113A>C
DNA change (hg38) -
Published as RBFOX1(NM_018723.3):c.1051A>C (p.(Thr351Pro))
ISCN -
DB-ID RBFOX1_000039
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) 0 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RBFOX1 NM_001142333.1 ?/. - c.970A>C r.(?) p.(Thr324Pro)
RBFOX1 NM_018723.3 ?/. - c.1051A>C r.(?) p.(Thr351Pro)


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