Variant #0000848813 (NC_000001.10:g.65312428G>A, NC_000001.10(NM_002227.2):c.1900-9C>T (JAK1))

Chromosome 1
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.65312428G>A
DNA change (hg38) -
Published as JAK1(NM_001321853.1):c.1900-9C>T
ISCN -
DB-ID JAK1_000024
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) 9.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
JAK1 NM_002227.2 -?/. - c.1900-9C>T r.(=) p.(=)
RAVER2 NM_018211.3 -?/. - c.*15760G>A r.(=) p.(=)


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