Variant #0001030305 (NC_000009.11:g.5073770G>T, NM_004972.3:c.1849G>T (JAK2))

Chromosome 9
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.5073770G>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID JAK2_000020 See all 4 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs77375493
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00036 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-04-10 12:09:01 +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     
JAK2 NM_004972.3 +/. - c.1849G>T r.(?) p.(Val617Phe)


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