Variant #0000720935 (NC_000006.11:g.41884564_41884565del, NM_004275.3:c.129_130del (MED20))

Chromosome 6
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.41884564_41884565del
DNA change (hg38) -
Published as MED20(NM_004275.4):c.129_130delTG (p.C43*)
ISCN -
DB-ID BYSL_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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BYSL NM_004053.3 ?/. - c.-4737_-4736del r.(?) p.(=)
MED20 NM_004275.3 ?/. - c.129_130del r.(?) p.(Cys43*)


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