Variant #0000807355 (NC_000016.9:g.3076765G>A, NM_024339.3:c.569G>A (THOC6))

Chromosome 16
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.3076765G>A
DNA change (hg38) -
Published as THOC6(NM_024339.4):c.569G>A (p.G190E), THOC6(NM_024339.5):c.569G>A (p.G190E)
ISCN -
DB-ID THOC6_000006 See all 5 reported entries
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) 0.00011 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 2021-09-17 14:40:49 +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.*4938G>A r.(=) p.(=)
HCFC1R1 NM_017885.2 +?/. - c.-2823C>T r.(?) p.(=)
THOC6 NM_024339.3 +?/. - c.569G>A r.(?) p.(Gly190Glu)


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