Variant #0000270684 (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 DCTN1(NM_004082.4):c.1484G>A (p.R495Q), DCTN1(NM_004082.5):c.1484G>A (p.R495Q)
ISCN -
DB-ID DCTN1_000015 See all 4 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) 0.01365 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DCTN1 NM_004082.4 -?/. - c.1484G>A r.(?) p.(Arg495Gln)


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