Variant #0000929539 (NC_000009.11:g.131021322G>A, NM_004408.2:c.*4329G>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.131021322G>A
DNA change (hg38) -
Published as GOLGA2(NM_004486.6):c.2056C>T (p.R686W)
ISCN -
DB-ID CIZ1_000054
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) 0.00152 View details
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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DNM1 NM_001288739.1 ?/. - c.*4329G>A r.(=) p.(=)
DNM1 NM_004408.2 ?/. - c.*4329G>A r.(=) p.(=)
GOLGA2 NM_004486.4 ?/. - c.2056C>T r.(?) p.(Arg686Trp)
CIZ1 NM_012127.2 ?/. - c.-54863C>T r.(?) p.(=)


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