Variant #0000316218 (NC_000001.10:g.11082411G>A, NM_007375.3:c.945G>A (TARDBP))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.11082411G>A
DNA change (hg38) g.11022354G>A
Published as TARDBP(NM_007375.3):c.945G>A (p.A315=)
ISCN -
DB-ID TARDBP_000149
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) 0.00015 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +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.*4531C>T r.(=) p.(=)
TARDBP NM_007375.3 -?/. - c.945G>A r.(?) p.(Ala315=)


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