Variant #0000605901 (NC_000001.10:g.65304232C>T, NM_002227.2:c.2883G>A (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.65304232C>T
DNA change (hg38) g.64838549C>T
Published as JAK1(NM_001321853.1):c.2883G>A (p.S961=)
ISCN -
DB-ID JAK1_000012
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) 7.0E-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 2019-12-04 14:54:23 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
JAK1 NM_002227.2 -?/. - c.2883G>A r.(?) p.(Ser961=)
RAVER2 NM_018211.3 -?/. - c.*7564C>T r.(=) p.(=)


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