Variant #0000690626 (NC_000010.10:g.101715473C>T, NM_015221.2:c.1758G>A (DNMBP))

Chromosome 10
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.101715473C>T
DNA change (hg38) -
Published as DNMBP(NM_015221.4):c.1758G>A (p.K586=)
ISCN -
DB-ID DNMBP_000013
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) 0.00048 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-09-15 15:50:26 +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     
DNMBP NM_015221.2 -?/. - c.1758G>A r.(?) p.(Lys586=)
DNMBP-AS1 NR_024130.2 -?/. - n.215C>T r.(?) -


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