Variant #0000974082 (NC_000001.10:g.65306997T>G, NM_002227.2:c.2580A>C (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.65306997T>G
DNA change (hg38) -
Published as JAK1(NM_002227.4):c.2580A>C (p.(Lys860Asn))
ISCN -
DB-ID JAK1_000029
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) 4.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:20:39 +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.2580A>C r.(?) p.(Lys860Asn)
RAVER2 NM_018211.3 -?/. - c.*10329T>G r.(=) p.(=)


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