Variant #0000883175 (NC_000001.10:g.225591082A>G, NM_002296.3:c.1771T>C (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.225591082A>G
DNA change (hg38) -
Published as LBR(NM_002296.4):c.1771T>C (p.C591R)
ISCN -
DB-ID DNAH14_000028
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 2022-11-01 13:01:21 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DNAH14 NM_001145154.1 ?/. - c.*379511A>G r.(=) p.(=)
DNAH14 NM_001373.1 ?/. - c.*4111A>G r.(=) p.(=)
LBR NM_002296.3 ?/. - c.1771T>C r.(?) p.(Cys591Arg)


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