Variant #0000910737 (NC_000001.10:g.11087386A>G, NM_007375.3:c.*4675A>G (TARDBP))

Chromosome 1
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.11087386A>G
DNA change (hg38) -
Published as MASP2(NM_006610.4):c.1617T>C (p.N539=)
ISCN -
DB-ID MASP2_000032
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) 0.00309 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-01-11 15:44:22 +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.1617T>C r.(?) p.(Asn539=)
TARDBP NM_007375.3 -/. - c.*4675A>G r.(=) p.(=)


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