Variant #0000997511 (NC_000009.11:g.131016966G>C, NM_004408.2:c.2568G>C (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.131016966G>C
DNA change (hg38) -
Published as DNM1(NM_001005336.1):c.*49G>C (p.?)
ISCN -
DB-ID CIZ1_000068
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +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.2568G>C r.(?) p.(Glu856Asp)
DNM1 NM_004408.2 ?/. - c.2568G>C r.(?) p.(Glu856Asp)
GOLGA2 NM_004486.4 ?/. - c.*2380C>G r.(=) p.(=)
CIZ1 NM_012127.2 ?/. - c.-50507C>G r.(?) p.(=)


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