Variant #0000653920 (NC_000001.10:g.225600341T>C, NM_002296.3:c.899A>G (LBR))

Chromosome 1
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.225600341T>C
DNA change (hg38) g.225412639T>C
Published as LBR(NM_002296.3):c.899A>G (p.(Tyr300Cys)), LBR(NM_194442.2):c.899A>G (p.Y300C)
ISCN -
DB-ID LBR_000026 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) 0.00058 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     
LBR NM_002296.3 ?/. - c.899A>G r.(?) p.(Tyr300Cys)


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