Variant #0000969503 (NC_000019.9:g.10829020C>A, NM_001005360.2:c.102C>A (DNM2))

Chromosome 19
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.10829020C>A
DNA change (hg38) -
Published as DNM2(NM_001005360.2):c.102C>A (p.I34=)
ISCN -
DB-ID QTRT1_000004
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2024-02-26 20:06:56 +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     
DNM2 NM_001005360.2 -?/. - c.102C>A r.(?) p.(=)
QTRT1 NM_031209.2 -?/. - c.*5074C>A r.(=) p.(=)


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