Variant #0000854482 (NC_000016.9:g.3080767C>T, NM_024339.3:c.*3109C>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.3080767C>T
DNA change (hg38) -
Published as BICDL2(NM_001103175.1):c.545G>A (p.R182Q)
ISCN -
DB-ID HCFC1R1_000005
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) 2.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:47:41 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HCFC1R1 NM_017885.2 ?/. - c.-6825G>A r.(?) p.(=)
THOC6 NM_024339.3 ?/. - c.*3109C>T r.(=) p.(=)


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