Variant #0000542850 (NC_000011.9:g.124750430C>A, NM_019055.5:c.*4357G>T (ROBO4))

Chromosome 11
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.124750430C>A
DNA change (hg38) g.124880534C>A
Published as ROBO3(NM_022370.3):c.4075C>A (p.R1359=)
ISCN -
DB-ID ROBO3_000032
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) 0.00029 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-01 16:19:11 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ROBO4 NM_019055.5 -?/. - c.*4357G>T r.(=) p.(=)
ROBO3 NM_022370.3 -?/. - c.4075C>A r.(?) p.(Arg1359=)


Screenscraping/webscraping (interacting with LOVD using scripts to download data) is strictly prohibited.
Use our APIs to retrieve data.