Variant #0000716674 (NC_000001.10:g.11087346_11087349del, NM_007375.3:c.*4635_*4638del (TARDBP))

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.11087346_11087349del
DNA change (hg38) -
Published as MASP2(NM_006610.3):c.1656_1659delTCTG (p.L553Qfs*9)
ISCN -
DB-ID MASP2_000028
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-02-08 18:36:18 +01:00 (CET)
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.1656_1659del r.(?) p.(Leu553Glnfs*9)
TARDBP NM_007375.3 ?/. - c.*4635_*4638del r.(=) p.(=)


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