Variant #0000855473 (NC_000019.9:g.16687499dup, NM_004831.3:c.1142dup (MED26))

Chromosome 19
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.16687499dup
DNA change (hg38) -
Published as MED26(NM_004831.3):c.1142dupG (p.S381Rfs*2)
ISCN -
DB-ID MED26_000005
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 2022-05-09 15:47:41 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MED26 NM_004831.3 ?/. - c.1142dup r.(?) p.(Ser381Argfs*2)
SLC35E1 NM_024881.4 ?/. - c.-4324dup r.(?) p.(=)


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