Variant #0000722277 (NC_000009.11:g.131013145G>A, NM_004408.2:c.2460G>A (DNM1))

Chromosome 9
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.131013145G>A
DNA change (hg38) -
Published as DNM1(NM_001288738.2):c.2460G>A (p.G820=)
ISCN -
DB-ID CIZ1_000023
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 2021-02-08 18:36:18 +01:00 (CET)
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.2460G>A r.(?) p.(Gly820=)
DNM1 NM_004408.2 ?/. - c.2460G>A r.(?) p.(Gly820=)
GOLGA2 NM_004486.4 ?/. - c.*6201C>T r.(=) p.(=)
CIZ1 NM_012127.2 ?/. - c.-46686C>T r.(?) p.(=)


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