Variant #0000856871 (NC_000001.10:g.11090237_11090241del, NM_007375.3:c.*7526_*7530del (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.11090237_11090241del
DNA change (hg38) -
Published as MASP2(NM_006610.4):c.1289_1293delGTGAG (p.C430Sfs*24)
ISCN -
DB-ID MASP2_000029
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-05-09 15:51:19 +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.1289_1293del r.(?) p.(Cys430Serfs*24)
TARDBP NM_007375.3 +?/. - c.*7526_*7530del r.(=) p.(=)


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