Variant #0000508224 (NC_000001.10:g.65339122G>A, NM_002227.2:c.414C>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.65339122G>A
DNA change (hg38) g.64873439G>A
Published as JAK1(NM_001321853.1):c.414C>T (p.Y138=), JAK1(NM_001321853.2):c.414C>T (p.Y138=)
ISCN -
DB-ID JAK1_000011 See all 2 reported entries
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) 0.00185 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +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.414C>T r.(?) p.(Tyr138=)
RAVER2 NM_018211.3 -?/. - c.*42454G>A r.(=) p.(=)


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