Variant #0000804962 (NC_000011.9:g.124749734T>G, NM_019055.5:c.*5053A>C (ROBO4))

Chromosome 11
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.124749734T>G
DNA change (hg38) -
Published as ROBO3(NM_022370.3):c.3848T>G (p.L1283R)
ISCN -
DB-ID ROBO3_000049
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) 2.0E-5 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 2021-09-17 14:40:49 +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     
ROBO4 NM_019055.5 ?/. - c.*5053A>C r.(=) p.(=)
ROBO3 NM_022370.3 ?/. - c.3848T>G r.(?) p.(Leu1283Arg)


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