Variant #0000623512 (NC_000016.9:g.69143500C>T, NM_001039690.3:c.*10828G>A (CHTF8))

Chromosome 16
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.69143500C>T
DNA change (hg38) g.69109597C>T
Published as HAS3(NM_001199280.1):c.202C>T (p.R68W)
ISCN -
DB-ID CHTF8_000001 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) 2.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-06 12:43:26 +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     
CHTF8 NM_001039690.3 ?/. - c.*10828G>A r.(=) p.(=)
HAS3 NM_138612.2 ?/. - c.202C>T r.(?) p.(Arg68Trp)


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