Variant #0000659516 (NC_000019.9:g.18710546A>G, NM_004750.4:c.226T>C (CRLF1))

Chromosome 19
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.18710546A>G
DNA change (hg38) g.18599736A>G
Published as -
ISCN -
DB-ID CRLF1_000051
Variant remarks -
Reference {Buers 2020: 31497877}
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 View details
Owner Insa Buers
Database submission license No license selected
Created by Insa Buers
Date created 2020-03-24 13:43:57 +01:00 (CET)
Date last edited 2020-07-15 16:10:09 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
CRLF1 NM_004750.4 +?/+? 2 c.226T>C r.(?) p.(Trp76Arg) -


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.