Variant #0001041061 (NC_000016.9:g.3075808C>T, NM_024339.3:c.139C>T (THOC6))

Chromosome 16
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.3075808C>T
DNA change (hg38) -
Published as THOC6(NM_024339.5):c.139C>T (p.(Gln47*))
ISCN -
DB-ID THOC6_000008 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 2025-05-05 21:14:00 +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     
TNFRSF12A NM_016639.2 +?/. - c.*3981C>T r.(=) p.(=)
HCFC1R1 NM_017885.2 +?/. - c.-1866G>A r.(?) p.(=)
THOC6 NM_024339.3 +?/. - c.139C>T r.(?) p.(Gln47*)


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