Variant #0000244043 (NC_000001.10:g.11003171C>T, NM_007375.3:c.(642C>T) (TARDBP))

Chromosome 1
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Effect unknown
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.11003171C>T
DNA change (hg38) g.10943114C>T
Published as -
ISCN -
DB-ID TARDBP_000148
Variant remarks Silent point mutation in coding region
Reference -
ClinVar ID -
dbSNP ID -
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Marc Cruts
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Julia Lopez
Date created 2013-05-01 13:44:57 +02:00 (CEST)
Date last edited 2018-11-09 14:00:33 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TARDBP NM_007375.3 -/? 5 c.(642C>T) r.(?) p.(=)


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