Variant #0000325172 (NC_000017.10:g.7788358_7788366del, NM_001005273.2:c.-3961_-3953del (CHD3))

Chromosome 17
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.7788358_7788366del
DNA change (hg38) g.7885040_7885048del
Published as CHD3(NM_001005271.3):c.234_242del (p.(Pro80_Pro82del))
ISCN -
DB-ID CHD3_000001
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CHD3 NM_001005273.2 -?/. - c.-3961_-3953del r.(?) p.(=)
LSMD1 NM_032356.3 -?/. - c.-27611_-27603del r.(?) p.(=)
CYB5D1 NM_144607.4 -?/. - c.*25428_*25436del r.(=) p.(=)


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