Variant #0000924595 (NC_000007.13:g.100240883G>A, NM_003227.3:c.-1751C>T (TFR2))

Chromosome 7
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.100240883G>A
DNA change (hg38) -
Published as ACTL6B(NM_016188.5):c.1267C>T (p.R423*)
ISCN -
DB-ID ACTL6B_000019
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-04-16 21:50:28 +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     
TFR2 NM_003227.3 +/. - c.-1751C>T r.(?) p.(=)
ACTL6B NM_016188.4 +/. - c.1267C>T r.(?) p.(Arg423*)


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