Variant #0000995762 (NC_000006.11:g.41884544C>A, NM_004275.3:c.148G>T (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>A
DNA change (hg38) -
Published as MED20(NM_004275.3):c.148G>T (p.(Ala50Ser)), MED20(NM_004275.4):c.148G>T (p.A50S)
ISCN -
DB-ID BYSL_000002 See all 2 reported entries
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) 0.0005 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BYSL NM_004053.3 -?/. - c.-4757C>A r.(?) p.(=)
MED20 NM_004275.3 -?/. - c.148G>T r.(?) p.(Ala50Ser)


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