Variant #0000693121 (NC_000022.10:g.22311807G>C, NM_003935.3:c.2268C>G (TOP3B))

Chromosome 22
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.22311807G>C
DNA change (hg38) -
Published as TOP3B(NM_003935.4):c.2268C>G (p.H756Q)
ISCN -
DB-ID PPM1F_000001
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_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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TOP3B NM_003935.3 -?/. - c.2268C>G r.(?) p.(His756Gln)
PPM1F NM_014634.3 -?/. - c.-4704C>G r.(?) p.(=)


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