Variant #0000516961 (NC_000002.11:g.74598723T>C, NM_004082.4:c.586A>G (DCTN1))

Chromosome 2
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.74598723T>C
DNA change (hg38) g.74371596T>C
Published as DCTN1(NM_004082.4):c.586A>G (p.I196V), DCTN1(NM_004082.5):c.586A>G (p.I196V)
ISCN -
DB-ID DCTN1_000067 See all 3 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) 0.0046 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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.586A>G r.(?) p.(Ile196Val)


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