Variant #0000281550 (NC_000019.9:g.17932190T>C, NM_000215.3:c.*5362A>G (JAK3))

Chromosome 19
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.17932190T>C
DNA change (hg38) g.17821381T>C
Published as INSL3(NM_001265587.2):c.126A>G (p.L42=)
ISCN -
DB-ID INSL3_000002
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) 0.304 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
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     
JAK3 NM_000215.3 -/. - c.*5362A>G r.(=) p.(=)
INSL3 NM_005543.3 -/. - c.126A>G r.(?) p.(Leu42=)


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