Variant #0000623443 (NC_000016.9:g.3076141T>A, NM_024339.3:c.298T>A (THOC6))

Chromosome 16
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.3076141T>A
DNA change (hg38) g.3026140T>A
Published as THOC6(NM_024339.4):c.298T>A (p.W100R), THOC6(NM_024339.5):c.298T>A (p.W100R)
ISCN -
DB-ID THOC6_000002 See all 7 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) 0.00017 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 2019-12-06 12:43:26 +01:00 (CET)
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.*4314T>A r.(=) p.(=)
HCFC1R1 NM_017885.2 +/. - c.-2199A>T r.(?) p.(=)
THOC6 NM_024339.3 +/. - c.298T>A r.(?) p.(Trp100Arg)


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