Variant #0001003760 (NC_000017.10:g.7788338C>T, NM_001005273.2:c.-3981C>T (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.7788338C>T
DNA change (hg38) -
Published as CHD3(NM_001005271.2):c.214C>T (p.(Leu72Phe))
ISCN -
DB-ID CHD3_000115
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 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CHD3 NM_001005273.2 -?/. - c.-3981C>T r.(?) p.(=)
LSMD1 NM_032356.3 -?/. - c.-27597G>A r.(?) p.(=)
CYB5D1 NM_144607.4 -?/. - c.*25408C>T r.(=) p.(=)


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