Variant #0000313764 (NC_000003.11:g.50380619C>A, RASSF1(NM_001206957.1):c.-2729G>T)

Chromosome 3
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.50380619C>A
DNA change (hg38) g.50343188C>A
Published as ZMYND10(NM_015896.3):c.529G>T (p.E177*)
ISCN -
DB-ID ZMYND10_000001
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RASSF1 NM_001206957.1 +/. - c.-2729G>T r.(?) p.(=)
NPRL2 NM_006545.4 +/. - c.*4418G>T r.(=) p.(=)
CYB561D2 NM_007022.3 +/. - c.-7888C>A r.(?) p.(=)
ZMYND10 NM_015896.2 +/. - c.529G>T r.(?) p.(Glu177Ter)