Variant #0000949330 (NC_000010.10:g.101989173G>A, NM_018294.4:c.*3811C>T (CWF19L1))

Chromosome 10
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.101989173G>A
DNA change (hg38) -
Published as CHUK(NM_001278.5):c.105+12C>T
ISCN -
DB-ID CHUK_000013
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) 0.00129 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-11-27 17:35:39 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CHUK NM_001278.3 -?/. - c.105+12C>T r.(=) p.(=)
CWF19L1 NM_018294.4 -?/. - c.*3811C>T r.(=) p.(=)


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