Variant #0001034181 (NC_000003.11:g.77089989G>A, NC_000003.11(NM_001128929.2):c.110-57176G>A (ROBO2))

Chromosome 3
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.77089989G>A
DNA change (hg38) -
Published as ROBO2(NM_001290039.2):c.53G>A (p.(Arg18Gln))
ISCN -
DB-ID ROBO2_000050
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 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +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     
ROBO2 NM_001128929.2 ?/. - c.110-57176G>A r.(=) p.(=)
ROBO2 NM_001395656.1 ?/. - c.53G>A r.(?) p.(Arg18Gln)


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