Variant #0000611876 (NC_000009.11:g.130965872C>A, NM_004408.2:c.123C>A (DNM1))

Chromosome 9
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.130965872C>A
DNA change (hg38) g.128203593C>A
Published as DNM1(NM_001288738.2):c.123C>A (p.S41R)
ISCN -
DB-ID CIZ1_000029
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DNM1 NM_001288739.1 +?/. - c.123C>A r.(?) p.(Ser41Arg)
DNM1 NM_004408.2 +?/. - c.123C>A r.(?) p.(Ser41Arg)
CIZ1 NM_012127.2 +?/. - c.-6+593G>T r.(=) p.(=)


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