Variant #0000608875 (NC_000003.11:g.77617558T>C, NM_001128929.2:c.1992T>C (ROBO2))

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.77617558T>C
DNA change (hg38) g.77568407T>C
Published as ROBO2(NM_001290040.1):c.1956T>C (p.T652=), ROBO2(NM_002942.5):c.1944T>C (p.T648=)
ISCN -
DB-ID ROBO2_000020 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) 0.00062 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 2019-12-04 14:54:23 +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     
ROBO2 NM_001128929.2 -?/. - c.1992T>C r.(?) p.(Thr664=)


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