Variant #0000037914 (NC_000019.9:g.18717401_18717403del, NM_004750.4:c.75_77del (CRLF1))

Chromosome 19
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.18717401_18717403del
DNA change (hg38) g.18606591_18606593del
Published as -
ISCN -
DB-ID CRLF1_000037
Variant remarks -
Reference PubMed: Piras 2014
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2014-06-27 20:03:51 +02:00 (CEST)
Date last edited 2020-07-15 16:10:12 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
CRLF1 NM_004750.4 -/. 1 c.75_77del r.(?) p.(Leu26del) -


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