Variant #0000659513 (NC_000019.9:g.18717489dup, NC_000019.9(NM_004750.4):c.23-45dup (CRLF1))

Chromosome 19
Allele Both (homozygous)
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.18717489dup
DNA change (hg38) -
Published as -
ISCN -
DB-ID CRLF1_000049
Variant remarks Variant Error [EMISMATCH/EINVALIDBOUNDARY]: This transcript variant has an error. Please fix this entry and then remove this message.
Reference PubMed: Buers 2020
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Insa Buers
Database submission license No license selected
Created by Insa Buers
Date created 2020-03-24 12:41:59 +01:00 (CET)
Date last edited 2020-03-24 13:19:14 +01:00 (CET)
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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.23-45dup r.? p.[Leu19Asnfs*32] -


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