Variant #0000520287 (NC_000003.11:g.50381254C>T, RASSF1(NM_001206957.1):c.-3364G>A)

Chromosome 3
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.50381254C>T
DNA change (hg38) g.50343823C>T
Published as ZMYND10(NM_015896.3):c.229G>A (p.A77T)
ISCN -
DB-ID CYB561D2_000002
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) 0.00114 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RASSF1 NM_001206957.1 -?/. - c.-3364G>A r.(?) p.(=)
NPRL2 NM_006545.4 -?/. - c.*3783G>A r.(=) p.(=)
CYB561D2 NM_007022.3 -?/. - c.-7253C>T r.(?) p.(=)
ZMYND10 NM_015896.2 -?/. - c.229G>A r.(?) p.(Ala77Thr)