Variant #0000620327 (NC_000001.10:g.11087642C>T, NM_007375.3:c.*4931C>T (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.11087642C>T
DNA change (hg38) g.11027585C>T
Published as MASP2(NM_006610.4):c.1361G>A (p.G454D)
ISCN -
DB-ID MASP2_000021
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_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     
MASP2 NM_006610.3 ?/. - c.1361G>A r.(?) p.(Gly454Asp)
TARDBP NM_007375.3 ?/. - c.*4931C>T r.(=) p.(=)


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