Variant #0000566629 (NC_000019.9:g.18707473dup, NM_004750.4:c.983dup (CRLF1))

Chromosome 19
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.18707473dup
DNA change (hg38) g.18596663dup
Published as CRLF1(NM_004750.5):c.983dupG (p.S328Rfs*2)
ISCN -
DB-ID CRLF1_000036 See all 3 reported entries
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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     

P-domain     
C19orf60 NM_001100418.1 +/. - c.*4483dup r.(?) p.(=) -
CRLF1 NM_004750.4 +/. - c.983dup r.(?) p.(Ser328ArgfsTer2) -


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