Variant #0000981150 (NC_000015.9:g.32929160del, NM_003020.3:c.-4827del (SCG5))

Chromosome 15
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.32929160del
DNA change (hg38) -
Published as ARHGAP11A(NM_014783.6):c.2186del (p.(Pro729GlnfsTer5))
ISCN -
DB-ID ARHGAP11A_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_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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SCG5 NM_003020.3 ?/. - c.-4827del r.(?) p.(=)
ARHGAP11A NM_014783.3 ?/. - c.2186del r.(?) p.(Pro729Glnfs*5)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.