Variant #0000930258 (NC_000014.8:g.102442034_102442037del, NC_000014.8(NM_001376.4):c.257-15_257-12del (DYNC1H1))

Chromosome 14
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.102442034_102442037del
DNA change (hg38) -
Published as DYNC1H1(NM_001376.5):c.257-15_257-12delTATT
ISCN -
DB-ID DYNC1H1_000380
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) Retrieve
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2023-07-07 10:10:56 +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     
DYNC1H1 NM_001376.4 -?/. - c.257-15_257-12del r.(=) p.(=)


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