Variant #0000655022 (NC_000003.11:g.78656062G>A, NM_002941.3:c.4565C>T (ROBO1))

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.78656062G>A
DNA change (hg38) g.78606912G>A
Published as ROBO1(NM_002941.4):c.4565C>T (p.S1522L), ROBO1(NM_133631.3):c.4430C>T (p.S1477L), ROBO1(NM_133631.4):c.4430C>T (p.S1477L)
ISCN -
DB-ID ROBO1_000008 See all 3 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) 0.00058 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 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2023-11-27 17:27:23 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ROBO1 NM_002941.3 ?/. - c.4565C>T r.(?) p.(Ser1522Leu)


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