Variant #0000677777 (NC_000006.11:g.41884544C>T, NM_004275.3:c.148G>A (MED20))

Chromosome 6
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.41884544C>T
DNA change (hg38) -
Published as MED20(NM_004275.4):c.148G>A (p.A50T)
ISCN -
DB-ID BYSL_000003
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) 0.00067 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 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2020-09-15 15:50:26 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BYSL NM_004053.3 -?/. - c.-4757C>T r.(?) p.(=)
MED20 NM_004275.3 -?/. - c.148G>A r.(?) p.(Ala50Thr)


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