Variant #0001031047 (NC_000001.10:g.11087465C>T, NM_007375.3:c.*4754C>T (TARDBP))

Chromosome 1
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.11087465C>T
DNA change (hg38) -
Published as MASP2(NM_006610.4):c.1538G>A (p.(Trp513*))
ISCN -
DB-ID MASP2_000038
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +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     
MASP2 NM_006610.3 +?/. - c.1538G>A r.(?) p.(Trp513*)
TARDBP NM_007375.3 +?/. - c.*4754C>T r.(=) p.(=)


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