Variant #0000984734 (NC_000023.10:g.50350728_50350729insCC, NM_020717.3:c.3413_3414insGG (SHROOM4))

Chromosome X
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.50350728_50350729insCC
DNA change (hg38) -
Published as SHROOM4(NM_020717.3):c.3413_3414insGG (p.E1140Kfs*42), SHROOM4(NM_020717.4):c.3413_3414insGG (p.(Glu1140LysfsTer42))
ISCN -
DB-ID SHROOM4_000081 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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +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     
SHROOM4 NM_020717.3 -?/. - c.3413_3414insGG r.(?) p.(Glu1140LysfsTer42)


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