Variant #0000557915 (NC_000016.9:g.3076725C>T, NM_024339.3:c.529C>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.3076725C>T
DNA change (hg38) g.3026724C>T
Published as THOC6(NM_024339.5):c.529C>T (p.R177W)
ISCN -
DB-ID HCFC1R1_000002
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) 3.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TNFRSF12A NM_016639.2 ?/. - c.*4898C>T r.(=) p.(=)
HCFC1R1 NM_017885.2 ?/. - c.-2783G>A r.(?) p.(=)
THOC6 NM_024339.3 ?/. - c.529C>T r.(?) p.(Arg177Trp)


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