Variant #0000913523 (NC_000011.9:g.124755116T>A, NM_019055.5:c.2822A>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.124755116T>A
DNA change (hg38) -
Published as ROBO4(NM_019055.6):c.2822A>T (p.D941V)
ISCN -
DB-ID ROBO3_000054
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) 0.00018 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-01-11 15:44:22 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ROBO4 NM_019055.5 -?/. - c.2822A>T r.(?) p.(Asp941Val)
ROBO3 NM_022370.3 -?/. - c.*3970T>A r.(=) p.(=)


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