Variant #0000527672 (NC_000006.11:g.15496915A>G, NM_004973.3:c.1459A>G (JARID2))

Chromosome 6
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.15496915A>G
DNA change (hg38) g.15496684A>G
Published as JARID2(NM_001267040.1):c.943A>G (p.(Lys315Glu)), JARID2(NM_004973.4):c.1459A>G (p.K487E)
ISCN -
DB-ID JARID2_000003 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) 0.00088 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 2019-07-18 18:22:55 +02:00 (CEST)
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     
JARID2 NM_004973.3 -?/. - c.1459A>G r.(?) p.(Lys487Glu)


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