Variant #0000557911 (NC_000016.9:g.3075704T>C, NC_000016.9(NM_024339.3):c.40-5T>C (THOC6))

Chromosome 16
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.3075704T>C
DNA change (hg38) g.3025703T>C
Published as THOC6(NM_001142350.1):c.40-5T>C (p.?)
ISCN -
DB-ID HCFC1R1_000001
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-09 11:12:13 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TNFRSF12A NM_016639.2 -?/. - c.*3877T>C r.(=) p.(=)
HCFC1R1 NM_017885.2 -?/. - c.-1762A>G r.(?) p.(=)
THOC6 NM_024339.3 -?/. - c.40-5T>C r.spl? p.?


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.