Variant #0000324392 (NC_000016.9:g.839702C>T, NM_022092.2:c.593C>T (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.839702C>T
DNA change (hg38) g.789702C>T
Published as CHTF18(NM_022092.2):c.593C>T (p.(Ala198Val))
ISCN -
DB-ID CHTF18_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) 0.0027 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GNG13 NM_016541.2 -?/. - c.*9017G>A r.(=) p.(=)
CHTF18 NM_022092.2 -?/. - c.593C>T r.(?) p.(Ala198Val)
RPUSD1 NM_058192.2 -?/. - c.-1454G>A r.(?) p.(=)


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