Variant #0000913087 (NC_000009.11:g.130988306G>A, NC_000009.11(NM_004408.2):c.1335+1638G>A (DNM1))

Chromosome 9
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.130988306G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID DNM1_000018 See all 11 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) 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 2023-01-11 15:44:22 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DNM1 NM_001288739.1 +/. - c.1197-8G>A r.(=) p.(=)
DNM1 NM_004408.2 +/. - c.1335+1638G>A r.(=) p.(=)
CIZ1 NM_012127.2 +/. - c.-21847C>T r.(?) p.(=)


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