Variant #0000870928 (NC_000010.10:g.104128551A>C, NM_004193.2:c.2932A>C (GBF1))

Chromosome 10
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method ACMG
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.104128551A>C
DNA change (hg38) g.102368794A>C
Published as -
ISCN -
DB-ID GBF1_000008
Variant remarks De novo variant
Reference -
ClinVar ID -
dbSNP ID -
Origin De novo
Segregation yes
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Gianina Ravenscroft
Database submission license Creative Commons Attribution-NonCommercial 4.0 InternationalCreative Commons License
Created by Gianina Ravenscroft
Date created 2022-06-22 17:19:28 +02:00 (CEST)
Date last edited 2024-06-24 16:56:22 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GBF1 NM_004193.2 +?/. - c.2932A>C r.(?) p.(Ile978Leu)



Screenings

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