Variant #0001002256 (NC_000016.9:g.3076749T>C, NM_024339.3:c.553T>C (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.3076749T>C
DNA change (hg38) -
Published as THOC6(NM_024339.3):c.553T>C (p.(Ser185Pro))
ISCN -
DB-ID HCFC1R1_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) 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     
TNFRSF12A NM_016639.2 ?/. - c.*4922T>C r.(=) p.(=)
HCFC1R1 NM_017885.2 ?/. - c.-2807A>G r.(?) p.(=)
THOC6 NM_024339.3 ?/. - c.553T>C r.(?) p.(Ser185Pro)


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