Variant #0000929538 (NC_000009.11:g.131001797G>A, NC_000009.11(NM_004408.2):c.1493+3G>A (DNM1))

Chromosome 9
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.131001797G>A
DNA change (hg38) -
Published as DNM1(NM_004408.4):c.1493+3G>A
ISCN -
DB-ID CIZ1_000053
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-07-07 10:10:56 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DNM1 NM_001288739.1 -?/. - c.1493+3G>A r.spl? p.?
DNM1 NM_004408.2 -?/. - c.1493+3G>A r.spl? p.?
CIZ1 NM_012127.2 -?/. - c.-35338C>T r.(?) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.