Variant #0000726733 (NC_000017.10:g.7788364_7788366dup, NM_001005273.2:c.-3955_-3953dup (CHD3))

Chromosome 17
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.7788364_7788366dup
DNA change (hg38) -
Published as CHD3(NM_001005271.2):c.240_242dupGCC (p.P82dup), CHD3(NM_001005271.3):c.240_242dupGCC (p.P82dup)
ISCN -
DB-ID CHD3_000011 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) 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 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2024-04-19 20:27:30 +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.-3955_-3953dup r.(?) p.(=)
LSMD1 NM_032356.3 -/. - c.-27605_-27603dup r.(?) p.(=)
CYB5D1 NM_144607.4 -/. - c.*25434_*25436dup r.(=) p.(=)


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