Variant #0000297705 (NC_000011.9:g.124750455_124750460del, NM_019055.5:c.*4334_*4339del (ROBO4))

Chromosome 11
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.124750455_124750460del
DNA change (hg38) g.124880559_124880564del
Published as ROBO3(NM_022370.4):c.4100_4105delGGAGTC (p.R1367_S1368del)
ISCN -
DB-ID ROBO3_000009
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ROBO4 NM_019055.5 -/. - c.*4334_*4339del r.(=) p.(=)
ROBO3 NM_022370.3 -/. - c.4100_4105del r.(?) p.(Arg1367_Ser1368del)


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