Variant #0001051413 (NC_000003.11:g.78685024C>T, NM_002941.3:c.3272G>A (ROBO1))

Chromosome 3
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.78685024C>T
DNA change (hg38) -
Published as ROBO1(NM_002941.4):c.3272G>A (p.(Ser1091Asn)), ROBO1(NM_133631.4):c.3137G>A (p.S1046N)
ISCN -
DB-ID ROBO1_000027 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) 0.03619 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 2025-11-01 13:22:20 +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     
ROBO1 NM_002941.3 -?/. - c.3272G>A r.(?) p.(Ser1091Asn)


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