Variant #0000536362 (NC_000009.11:g.130982582C>T, NM_004408.2:c.811C>T (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.130982582C>T
DNA change (hg38) g.128220303C>T
Published as -
ISCN -
DB-ID CIZ1_000015
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
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     
DNM1 NM_001288739.1 +?/. - c.811C>T r.(?) p.(Arg271Cys)
DNM1 NM_004408.2 +?/. - c.811C>T r.(?) p.(Arg271Cys)
CIZ1 NM_012127.2 +?/. - c.-16123G>A r.(?) p.(=)


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