Variant #0001055301 (NC_000016.9:g.840351G>A, NM_022092.2:c.704G>A (CHTF18))

Chromosome 16
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.840351G>A
DNA change (hg38) -
Published as CHTF18(NM_022092.3):c.704G>A (p.(Arg235Gln))
ISCN -
DB-ID CHTF18_000023
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) 7.0E-5 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 2025-11-01 13:22:20 +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     
GNG13 NM_016541.2 -?/. - c.*8368C>T r.(=) p.(=)
CHTF18 NM_022092.2 -?/. - c.704G>A r.(?) p.(Arg235Gln)
RPUSD1 NM_058192.2 -?/. - c.-2103C>T r.(?) p.(=)


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