Variant #0000996625 (NC_000007.13:g.66098412C>T, NM_153033.4:c.295C>T (KCTD7))

Chromosome 7
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.66098412C>T
DNA change (hg38) -
Published as KCTD7(NM_153033.4):c.295C>T (p.(Arg99*)), KCTD7(NM_153033.5):c.295C>T (p.R99*)
ISCN -
DB-ID KCTD7_000005 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) 0 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 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     
KCTD7 NM_153033.4 +/. - c.295C>T r.(?) p.(Arg99Ter)


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