Variant #0000914126 (NC_000014.8:g.102494175G>A, NC_000014.8(NM_001376.4):c.9263+5G>A (DYNC1H1))

Chromosome 14
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.102494175G>A
DNA change (hg38) -
Published as DYNC1H1(NM_001376.4):c.9263+5G>A (p.?), DYNC1H1(NM_001376.5):c.9263+5G>A
ISCN -
DB-ID DYNC1H1_000233 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) 4.0E-5 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 2023-01-11 15:44:22 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DYNC1H1 NM_001376.4 ?/. - c.9263+5G>A r.spl? p.?


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