Variant #0001041060 (NC_000016.9:g.3075807G>T, NM_024339.3:c.138G>T (THOC6))

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.3075807G>T
DNA change (hg38) -
Published as THOC6(NM_024339.5):c.138G>T (p.(Gly46=))
ISCN -
DB-ID HCFC1R1_000007
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.*3980G>T r.(=) p.(=)
HCFC1R1 NM_017885.2 ?/. - c.-1865C>A r.(?) p.(=)
THOC6 NM_024339.3 ?/. - c.138G>T r.(?) p.(=)


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