Variant #0000887102 (NC_000006.11:g.15496856_15496881del, NM_004973.3:c.1400_1425del (JARID2))

Chromosome 6
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.15496856_15496881del
DNA change (hg38) -
Published as JARID2(NM_004973.4):c.1400_1425delCCGAAGGCCCTGGCAAGAAGGCCCCG (p.A467Gfs*48)
ISCN -
DB-ID JARID2_000007
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) Retrieve
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2022-11-01 13:01:21 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
JARID2 NM_004973.3 +/. - c.1400_1425del r.(?) p.(Ala467Glyfs*48)


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