Variant #0000922910 (NC_000001.10:g.11087272T>G, NM_007375.3:c.*4561T>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.11087272T>G
DNA change (hg38) -
Published as MASP2(NM_006610.4):c.1731A>C (p.Q577H)
ISCN -
DB-ID MASP2_000022 See all 2 reported entries
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) 0.00398 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 2023-04-16 21:50:28 +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.1731A>C r.(?) p.(Gln577His)
TARDBP NM_007375.3 -/. - c.*4561T>G r.(=) p.(=)


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