Variant #0001037360 (NC_000009.11:g.139889289C>T, NM_183241.1:c.*1032C>T (C9orf142))

Chromosome 9
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.139889289C>T
DNA change (hg38) -
Published as CLIC3(NM_004669.3):c.555G>A (p.(Thr185=))
ISCN -
DB-ID C9orf142_000006
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 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CLIC3 NM_004669.2 ?/. - c.555G>A r.(?) p.(=)
C9orf142 NM_183241.1 ?/. - c.*1032C>T r.(=) p.(=)


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