Variant #0000038075 (NC_000002.11:g.74596527C>T, NM_004082.4:c.1484G>A (DCTN1))

Chromosome 2
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.74596527C>T
DNA change (hg38) g.74369400C>T
Published as G2284A
ISCN -
DB-ID DCTN1_000015 See all 4 reported entries
Variant remarks found in 5/250 ALS patients, 3/150 controls
Reference PubMed: Munch 2004
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency 8/400 individuals
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.01365 View details
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2014-07-11 14:05:28 +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     
DCTN1 NM_004082.4 -?/. 13 c.1484G>A r.(?) p.(Arg495Gln)


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