Variant #0000314378 (NC_000001.10:g.11082349G>T, NM_007375.3:c.883G>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.11082349G>T
DNA change (hg38) g.11022292G>T
Published as TARDBP(NM_007375.3):c.883G>T (p.G295C)
ISCN -
DB-ID TARDBP_000008 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) Retrieve
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MASP2 NM_006610.3 ?/. - c.*4593C>A r.(=) p.(=)
TARDBP NM_007375.3 ?/. - c.883G>T r.(?) p.(Gly295Cys)


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